Every recall we track for Hospira a Pfizer Company — 4 in all, all from 2017 — plus the complaints and injury reports the public filed about them.
4 recalls from Hospira a Pfizer Company are on record with U.S. safety agencies, from 2017.
Hospira a Pfizer Company recalls 8.4% Sodium Bicarbonate Inj., USP 50 mL Single-dose, 50 mEq (1 mEq/mL) 4.2 grams (84 mg/mL), Rx Only, Mfd by Hospira,, dated Jun 15, 2017. Every Hospira a Pfizer Company recall is listed on this page, newest first.
The most common reasons on record: Lack of Sterility Assurance (4).
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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