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   <title>Form  6-K        Grifols SA                For: Jun 18</title>
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   <pubDate>Thu, 18 Jun 2026 16:00:00 -0400</pubDate>
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   <title>Form  6-K        Grifols SA                For: Jun 18</title>
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   <title>Form  6-K        Grifols SA                For: Jun 18</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Grifols+SA++++++++++++++++For%3A+Jun+18/26665768.html</link>
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   <title>Grifols launches FESILTY fibrinogen concentrate in the US</title>
   <link>http://www.streetinsider.com/Corporate+News/Grifols+launches+FESILTY+fibrinogen+concentrate+in+the+US/26644496.html</link>
   <description>&lt;p&gt;Grifols (MCE: GRF, NASDAQ: GRFS) announced the US launch of FESILTY, a fibrinogen concentrate approved by the Food and Drug Administration for treating acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency.&lt;/p&gt;&lt;p&gt;The FDA approved FESILTY in December for patients with congenital fibrinogen deficiency, including hypo- or afibrinogenemia, but not for dysfibrinogenemia. The treatment addresses a rare inherited condition caused by genetic mutations that impair fibrinogen production or function.&lt;/p&gt;&lt;p&gt;FESILTY provides a purified fibrinogen concentrate that enables rapid restoration of fibrinogen levels during bleeding events. The product can be stored at room temperature and reconstituted in approximately three minutes,</description>
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   <title>Grifols launches FESILTY fibrinogen concentrate in the US</title>
   <link>http://www.streetinsider.com/Corporate+News/Grifols+launches+FESILTY+fibrinogen+concentrate+in+the+US/26644496.html</link>
   <description>&lt;p&gt;Grifols (MCE: GRF, NASDAQ: GRFS) announced the US launch of FESILTY, a fibrinogen concentrate approved by the Food and Drug Administration for treating acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency.&lt;/p&gt;&lt;p&gt;The FDA approved FESILTY in December for patients with congenital fibrinogen deficiency, including hypo- or afibrinogenemia, but not for dysfibrinogenemia. The treatment addresses a rare inherited condition caused by genetic mutations that impair fibrinogen production or function.&lt;/p&gt;&lt;p&gt;FESILTY provides a purified fibrinogen concentrate that enables rapid restoration of fibrinogen levels during bleeding events. The product can be stored at room temperature and reconstituted in approximately three minutes,</description>
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   <title>Grifols launches FESILTY fibrinogen concentrate in the US</title>
   <link>http://www.streetinsider.com/Corporate+News/Grifols+launches+FESILTY+fibrinogen+concentrate+in+the+US/26644496.html</link>
   <description>&lt;p&gt;Grifols (MCE: GRF, NASDAQ: GRFS) announced the US launch of FESILTY, a fibrinogen concentrate approved by the Food and Drug Administration for treating acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency.&lt;/p&gt;&lt;p&gt;The FDA approved FESILTY in December for patients with congenital fibrinogen deficiency, including hypo- or afibrinogenemia, but not for dysfibrinogenemia. The treatment addresses a rare inherited condition caused by genetic mutations that impair fibrinogen production or function.&lt;/p&gt;&lt;p&gt;FESILTY provides a purified fibrinogen concentrate that enables rapid restoration of fibrinogen levels during bleeding events. The product can be stored at room temperature and reconstituted in approximately three minutes,</description>
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   <title>Grifols launches FESILTY fibrinogen concentrate in the US</title>
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   <description>&lt;p&gt;Grifols (MCE: GRF, NASDAQ: GRFS) announced the US launch of FESILTY, a fibrinogen concentrate approved by the Food and Drug Administration for treating acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency.&lt;/p&gt;&lt;p&gt;The FDA approved FESILTY in December for patients with congenital fibrinogen deficiency, including hypo- or afibrinogenemia, but not for dysfibrinogenemia. The treatment addresses a rare inherited condition caused by genetic mutations that impair fibrinogen production or function.&lt;/p&gt;&lt;p&gt;FESILTY provides a purified fibrinogen concentrate that enables rapid restoration of fibrinogen levels during bleeding events. The product can be stored at room temperature and reconstituted in approximately three minutes,</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
   <link>http://www.streetinsider.com/Press+Releases/Grifols+Launches+FESILTY%E2%84%A2+%28fibrinogen%2C+human-chmt%29+in+the+U.S./26644416.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
   <link>http://www.streetinsider.com/Press+Releases/Grifols+Launches+FESILTY%E2%84%A2+%28fibrinogen%2C+human-chmt%29+in+the+U.S./26644416.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
   <link>http://www.streetinsider.com/Press+Releases/Grifols+Launches+FESILTY%E2%84%A2+%28fibrinogen%2C+human-chmt%29+in+the+U.S./26644416.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
   <link>http://www.streetinsider.com/Press+Releases/Grifols+Launches+FESILTY%E2%84%A2+%28fibrinogen%2C+human-chmt%29+in+the+U.S./26644416.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
   <link>http://www.streetinsider.com/Press+Releases/Grifols+Launches+FESILTY%E2%84%A2+%28fibrinogen%2C+human-chmt%29+in+the+U.S./26644416.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
   <link>http://www.streetinsider.com/Press+Releases/Grifols+Launches+FESILTY%E2%84%A2+%28fibrinogen%2C+human-chmt%29+in+the+U.S./26644416.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Grifols+Launches+FESILTY%E2%84%A2+%28fibrinogen%2C+human-chmt%29+in+the+U.S./26644416.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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   <title>Grifols Launches FESILTY™ (fibrinogen, human-chmt) in the U.S.</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Grifols+Launches+FESILTY%E2%84%A2+%28fibrinogen%2C+human-chmt%29+in+the+U.S./26644416.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;strong&gt;&lt;em&gt;The new fibrinogen concentrate, approved in the U.S. for acute bleeding episodes in pediatric and adult patients with congenital fibrinogen deficiency, is now available in the U.S.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;li style=&quot;text-align:justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;FESILTY complements Grifols’ bleeding management portfolio, expanding therapeutic options for patients.&lt;/em&gt;&lt;/strong&gt;&lt;br&gt;&lt;/br&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p align=&quot;justify&quot;&gt;BARCELONA, Spain, June  15, 2026  (GLOBE NEWSWIRE) -- Grifols (MCE:GRF, MCE:GRF.P, NASDAQ:GRFS), a global healthcare company and leading producer of plasma-derived medicines, today announced the U.S. launch of its new fibrinogen concentrate. Approved by the U.S. Food and Drug Administration in December for the treatment of acute bleeding episodes in pediatric and adult patients with congenital fibrinogen</description>
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