FDA recall record

PharMEDium Services HYDROmorphone in 0.9% Sodium Chloride HCl, 1 mg per mL, For IV Use, 30 recall — FDA D-1084-2020

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

Class IIclassification
D-1084-2020official record ID
Apr 15, 2020report date

Recall record at a glance

Official recordD-1084-2020
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPharMEDium Services, LLC
Report dateApr 15, 2020
Recall initiation dateMar 16, 2020
Quantity1840 units
LocationDayton, NJ, United States

Official product description

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

Why the product was recalled

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

Distribution information

Distributed Nationwide in the US

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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