US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 13, 2017 (9 years ago)

Hydromorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride Injection 1 mL, packaged in…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Superpotent drug: out of specification result for potency

What was recalled

Hydromorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride Injection 1 mL, packaged in syringes, Rx Only , PharMEDium Services, LLC. 913 N. Davis Ave Cleveland, MS 38732, NDC 61553-352-40

Recalling firm
PharMEDium Services, LLC.
NDC code
61553-352-40
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0080-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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