FDA recall record

Oxycodone Hydrochloride Oral Solution, USP 5 mg/5mL unit dose cups recall — FDA D-0231-2021

Presence of Foreign Substance: Particulate matter was found in multiple lots of product.

Class IIIclassification
D-0231-2021official record ID
Jan 20, 2021report date

Recall record at a glance

Official recordD-0231-2021
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmGenus Lifesciences Inc.
Report dateJan 20, 2021
Recall initiation dateDec 23, 2020
Quantity1,171,550 cups
LocationAllentown, PA, United States

Official product description

Oxycodone Hydrochloride Oral Solution, USP 5 mg/5mL unit dose cups, Rx Only, Genus Lifesciences Inc. NDC 64950-354-05 Case NDC: 64950-354-450(40 unit dose cups) Case NDC 64950-354-55 (50 unit dose cups)

Why the product was recalled

Presence of Foreign Substance: Particulate matter was found in multiple lots of product.

Distribution information

Distributed Nationwide in the USA

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement 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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