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Hospira Recalls Buprenorphine, Labetalol Injectables Due to Packaging Defect

Hospira Inc Issues A Voluntary Nationwide Recall For Buprenorphine Hydrochloride Injection CarpujectTM Units and Labetalol Hydrochloride Injection, USP CarpujectTM Units Due to the Potential for Incomplete Crimp Seals

Hospira Inc Issues A Voluntary Nationwide Recall For Buprenorphine Hydrochloride Injection CarpujectTM Units and Labetalol Hydrochloride Injection, USP CarpujectTM Units Due to the Potential for Incomplete Crimp Seals
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Pfizer : Hospira Inc Issues A Voluntary Nationwide Recall For Buprenorphine Hydrochloride Injection Carpuject™ Units and Labetalol Hydrochloride Injection, USP Carpuject™ Units Due To The Potential For Incomplete Crimp Seals

FOR IMMEDIATE RELEASE - May 21, 2024 - NEW YORK, NY., Hospira, Inc., a Pfizer company , is voluntarily recalling the lots listed in the table below of Buprenorphine Hydrochloride Injection CarpujectTM.

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