PlainRecalls
FDA Drug Moderate Class II Ongoing

Ketorolac Tromethamine Ophthalmic Solution, 0.5%, 10 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9, Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-1003-2

Reported: July 2, 2025 Initiated: May 28, 2025 #D-0494-2025

Product Description

Ketorolac Tromethamine Ophthalmic Solution, 0.5%, 10 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9, Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-1003-2

Reason for Recall

Lack of Assurance of Sterility

Details

Recalling Firm
Apotex Corp.
Units Affected
87,840 bottles
Distribution
US Nationwide.
Location
Weston, FL

Frequently Asked Questions

What product was recalled?
Ketorolac Tromethamine Ophthalmic Solution, 0.5%, 10 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9, Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-1003-2. Recalled by Apotex Corp.. Units affected: 87,840 bottles.
Why was this product recalled?
Lack of Assurance of Sterility
Which agency issued this recall?
This recall was issued by the FDA Drug on July 2, 2025. Severity: Moderate. Recall number: D-0494-2025.