FDA recall record

Apotex Timolol Maleate Ophthalmic Solution, USP 0.5%, 2.5 mL recall — FDA D-0093-2023

Failed Stability Specifications: Out of specification for weight loss at the 18-month stability timepoint and projected weight loss of 21.1% at shelf life.

Class IIIclassification
D-0093-2023official record ID
Jan 4, 2023report date

Recall record at a glance

Official recordD-0093-2023
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmApotex Corp.
Report dateJan 4, 2023
Recall initiation dateDec 21, 2022
Quantity22,027 bottles
LocationWeston, FL, United States

Official product description

Timolol Maleate Ophthalmic Solution, USP 0.5%, 2.5 mL, Rx Only, Mfg by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Mfg for: Apotex Corp. Weston, FL 33326, NDC 60505-1005-4

Why the product was recalled

Failed Stability Specifications: Out of specification for weight loss at the 18-month stability timepoint and projected weight loss of 21.1% at shelf life.

Distribution information

USA Nationwide

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

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