Reported May 22, 2024 · Announced

Hospira Inc. recalls Hospira Buprenorphine Hydrochloride Injection Carpuject Units and Labetalol Hydrochloride Injection, USP Carpuject Units due to Device &…

Hospira Inc.

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

What you should do

Stop using the product and follow the return or refund instructions in the firm's announcement.

Is this the product you have?

  • Buprenorphine Hydrochloride Injection Carpuject Units and Labetalol Hydrochloride Injection
  • USP Carpuject Units BrandHospira. Animal & Veterinary, Drugs

Why it was recalled

Device & Drug Safety – Potential Packaging Defect

The agency has not ranked the risk yet — treat the notice as a caution.

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Where this came from

Source: U.S. Food & Drug Administration

Read the FDA (recalls & safety alerts) notice

Data as of Sep 19, 5:07 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.