FDA recall record

Teva Pharmaceuticals USA Penicillin V Potassium for Oral Solution, USP 125 mg (200,000 U) recall — FDA D-0294-2022

Subpotent

Class IIclassification
D-0294-2022official record ID
Dec 29, 2021report date

Recall record at a glance

Official recordD-0294-2022
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTeva Pharmaceuticals USA
Report dateDec 29, 2021
Recall initiation dateDec 16, 2021
Quantitya) 86,790 and b) 25,416 bottles
LocationParsippany, NJ, United States

Official product description

Penicillin V Potassium for Oral Solution, USP 125 mg (200,000 U) per 5 mL a) 100 mL (NDC 00093-4125-73) and b) 200 mL (NDC 00093-4125-74) (when mixed) bottles, Rx Only, Manufactured For: Teva Pharmaceuticals USA, Inc. North Wales, PA 19454

Why the product was recalled

Subpotent

Distribution information

nationwide

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

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