Hospira Inc., A Pfizer Company
Lake Forest, IL, United States
This page shows every FDA and USDA recall linked to Hospira Inc., A Pfizer Company. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
8
Total Recalls
2016
First Recall
2017
Most Recent
2
Class I (Most Serious)
Drug: 6
Device: 2
Class II: 3
Class III: 1
Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 5 mL Single-use vial, Rx Only, Sterile, Manufactured by: Glan...
Jul 26, 2017
· Drug
Class III
Terminated
Levophed norepinephrine bitartrate, injection, USP, 4 mg /4 mL (1 mg/mL),Rx only, Hospira, Inc. Lake Forest,...
Jun 21, 2017
· Drug
Class II
Terminated
Vancomycin Hydrochloride for Injection, USP, 10 grams, Pharmacy Bulk Package - Not For Direct Infusion, For In...
Apr 12, 2017
· Drug
Class I
Terminated
METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, H...
Mar 1, 2017
· Drug
Class II
Terminated
Plum 360 Infusion Pump, Software Version 15.02. The infusion pump is capable of delivering fluids for a variet...
Dec 30, 2016
· Device
Terminated
Bupivacaine Hydrochloride Inj., USP (2.5 mg/mL) 0.25%, packaged in 30 mL Single-dose Preservative-Free vials,...
Dec 28, 2016
· Drug
Class I
Ongoing
Marcaine 0.5% (bupivacaine HCl) injection, USP, 250 mg/50 mL (5 mg/mL), 50 mL Multiple-Dose Vial, Rx only, Hos...
Oct 19, 2016
· Drug
Class II
Terminated
Hospira MedNet Medication Management Suite software, version 6.1, List Numbers 16037-64-02 and 16037-64-03, in...
Jul 28, 2016
· Device
Terminated