US Drug Recall Register
Class I · High risk Terminated Initiated Jun 7, 2019 (7 years ago)

Hydromorphone HCl in 0.9% sodium chloride, 0.5mg per mL, 1 mL in 3mL BD Syringe…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Incorrect Product Formulation; Firm's customer resource center (CRC) statement indicates that the product is sulfite free, however the product is produced with a raw material that contains sulfite

What was recalled

Hydromorphone HCl in 0.9% sodium chloride, 0.5mg per mL, 1 mL in 3mL BD Syringe, PharMEDium 913 N Davis Ave Cleveland, MS 38732, 800-523-7749, NDC 61553-352-78

Recalling firm
PharMEDium Services, LLC
NDC code
61553-352-78
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1488-2019

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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