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Urgent: Recall Issued For Treprostinil Injection Due To Silicone Contamination

Par Pharmaceutical's Canva Endo International initiates recall for Treprostinil Injection lot over silicone particulates issue. Learn why silicone in injectables can pose health risks and what actions to take for safety. Check if your Treprostinil 20mg/20mL Injection belongs to the affected Lot 57014. Stay informed for your well-being.

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Recalled Blood Pressure Meds In Michigan Could Lead To Death

Recalled Blood Pressure Meds In Michigan Could Lead To Death
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Recalled Blood Pressure Meds In Michigan Could Lead To Death

Recalled Blood Pressure Meds In Michigan Could Lead To Death
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Par Pharmaceutical Issues Voluntary Nationwide Recall of Seven Lots of Treprostinil Injection Due to Potential for Silicone Particulates in the Product Solution

Par Pharmaceutical Issues Voluntary Nationwide Recall of Seven Lots of Treprostinil Injection Due to Potential for Silicone Particulates in the Product Solution
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Par Pharmaceutical Issues Voluntary Nationwide Recall of One Lot of Treprostinil Injection Due to Potential for Silicone Particulates in the Product Solution

Endo International plc announced today that one of its operating companies, Par Pharmaceutical, Inc. (Par), is voluntarily recalling one lot of Treprostinil Injection 20mg/20mL (1mg/mL) to the consumer level. The product is being recalled due to the potential for the presence of silicone particulate

Linda hussCompany nameWinmar incCompany contact informationDrug administrationEndo internationalCompany announcementAnnouncement dateSilicone particulatePar pharmaceuticalTreprostinil injectionWatch adverse event reporting