Every recall we track for Hospira Inc. A Pfizer Company — 8 in all, from 2016–2018 — plus the complaints and injury reports the public filed about them.
Recalls on record by year — 8 drug.
8 recalls from Hospira Inc. A Pfizer Company are on record with U.S. safety agencies, from 2016–2018.
Hospira Inc. A Pfizer Company recalls Labetalol Hydrochloride Injection, USP, 100 mg/ 20 mL (5 mg/mL), 20 mL Multidose Vial, Rx only, labeled as a) Hospira,, dated Feb 20, 2018. Every Hospira Inc. A Pfizer Company recall is listed on this page, newest first.
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
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