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Drug recall · FDA · Published February 20, 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,

Defective Container: Cracked glass at the rim surface of glass vials, covered by the stopper and crimp seal.

🇺🇸 FDA recall #D-0576-2018DrugHospira Inc. A Pfizer Company ›
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Recalling firmHospira Inc. A Pfizer Company1776 Centennial Dr, N/A · Mcpherson, KS 67460-9301
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
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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

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“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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  • Brand
    Hospira Inc. A Pfizer Company
  • Category
    Drug
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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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA