Hospira Inc., A Pfizer Company: 9 recalls on record

Recalls filed with 1 agency: FDA (9).

First recall on record: September 21, 2016. Most recent: March 14, 2018.

Risk classification: Class I: 2 · Class II: 6 · Class III: 1

Most recent recalls

DateAgencyProduct
March 14, 2018FDALabetalol Hydrochloride Injection, USP, 100 mg/ 20 mL (5 mg/mL), 20 mL Multidose Vial, Rx…D-0576-2018
July 26, 2017FDAArgatroban Injection, 250 mg/2.5 mL (100 mg/mL), 5 mL Single-use vial, Rx Only, Sterile, …D-0980-2017
June 21, 2017FDALevophed norepinephrine bitartrate, injection, USP, 4 mg /4 mL (1 mg/mL),Rx only, Hospir…D-0898-2017
April 12, 2017FDAVancomycin Hydrochloride for Injection, USP, 10 grams, Pharmacy Bulk Package - Not For Di…D-0638-2017
April 5, 2017FDAPlum 360 Infusion Pump, Software Version 15.02. The infusion pump is capable of deliverin…Z-1682-2017
March 1, 2017FDAMETRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, R…D-0480-2017
December 28, 2016FDABupivacaine Hydrochloride Inj., USP (2.5 mg/mL) 0.25%, packaged in 30 mL Single-dose Pres…D-0218-2017
October 19, 2016FDAMarcaine 0.25% (bupivacaine HCl) injection, USP, 125 mg/50 mL (2.5 mg/mL), 50 mL Multiple…D-0096-2017
September 21, 2016FDAHospira MedNet Medication Management Suite software, version 6.1, List Numbers 16037-64-0…Z-2790-2016

Questions about this company

How many recalls does Hospira Inc., A Pfizer Company have?
Recalert has 9 U.S. recalls on record for Hospira Inc., A Pfizer Company, published between September 21, 2016 and March 14, 2018.
What was the most recent Hospira Inc., A Pfizer Company recall?
FDA recall D-0576-2018, published March 14, 2018: Labetalol Hydrochloride Injection, USP, 100 mg/ 20 mL (5 mg/mL), 20 mL Multidose Vial, Rx only, labeled as a) Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2267-20; and b) NOVAPLUS, Manufactured by …
Which agencies have handled Hospira Inc., A Pfizer Company recalls?
Hospira Inc., A Pfizer Company appears as the recalling firm in recalls from: FDA (9).

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