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,
Defective Container: Cracked glass at the rim surface of glass vials, covered by the stopper and crimp seal.
Recall notice
Defective Container: Cracked glass at the rim surface of glass vials, covered by the stopper and crimp seal.
Contact the company & request your remedy
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We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
Source Page by GovInfoNow · govinfonow.com/recall/40805-hospira-inc-a-pfizer-company-recalls-labetalol-hydrochloride-injection-usp · Recall date February 20, 2018 · FDA enforcement record: FDA #D-0576-2018
Cite this page
“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,.” GovInfoNow, recall dated February 20, 2018. https://govinfonow.com/recall/40805-hospira-inc-a-pfizer-company-recalls-labetalol-hydrochloride-injection-usp. Based on FDA recall #D-0576-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0576-2018%22&limit=1).
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Contact Hospira Inc. A Pfizer Company
We’ve drafted a message you can send Hospira Inc. A Pfizer Company to request your refund or repair — edit it as you like.
Subject: Recall D-0576-2018 — Hospira Inc. A Pfizer Company Hospira Inc. A Pfizer Company recalls Labetalol Hydrochloride Injecti Hello, I own a 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, that is covered by recall D-0576-2018 from Hospira Inc. A Pfizer Company. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0576-2018 (February 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0576-2018 to see it in context.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
