US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 15, 2025 (17 months ago)

HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL), packaged in a 50 mL Cassette, Rx Only…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Superpotent Drug: Assay/potency result for hydromorphone HCl in the compounded stability lot was higher than specification..

What was recalled

HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL), packaged in a 50 mL Cassette, Rx Only, OurPharma, LLC, 2512 S. City Lake Rd., Fayetteville, AR 72701, NDC 73013-1040-01.

Recalling firm
OurPharma LLC
NDC code
73013-1040-01
Origin
AR, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0385-2025

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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