FDA recall record

Paxil CR, Paroxetine, Extended-Release Tablets, 37.5mg, 30 count bottle recall — FDA D-0804-2026

Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteria

Class IIclassification
D-0804-2026official record ID
Sep 2, 2026report date

Recall record at a glance

Official recordD-0804-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmApotex Corp.
Report dateSep 2, 2026
Recall initiation dateAug 13, 2026
Quantity6,972 bottles
LocationWeston, FL, United States

Official product description

Paxil CR, Paroxetine, Extended-Release Tablets, 37.5mg, 30 count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-4379-3

Why the product was recalled

Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteria

Distribution information

US 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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