US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 16, 2020 (6 years ago)

HYDROmorphone in 0.9% Sodium Chloride HCl, 1 mg per mL, For IV Use, 30 mg per 30 mL, 30…

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

Why it was recalled

Firm is recalling 46 lots of various products because of a lack of sterility assurance.

What was recalled

HYDROmorphone in 0.9% Sodium Chloride HCl, 1 mg per mL, For IV Use, 30 mg per 30 mL, 30 mL in a 35 mL Monoject Barrel Syringe, PharMEDium Services LLC 913 M. Davis Ave Cleveland, MS. NDC 61553-166-44

Recalling firm
PharMEDium Services, LLC
NDC code
61553-166-44
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1084-2020

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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