Pharmedium Services, LLC recalls HYDROmorphone HCl Injection in all strengths, all doses, and all packaging.
- Recall date
- December 27, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0433-2018
- FDA classification
- Class II
- Brand / firm
- Pharmedium Services, LLC
- Sold / distributed
- U.S.A. Nationwide
Why it was recalled
Lack of sterility assurance.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
HYDROmorphone HCl Injection in all strengths, all doses, and all packaging.
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