Apotex recalls Ketorolac 0.5% eye drops due to lack of sterility assurance. This could cause infections. Check NDC 60505-1003-2, batch TZ1236, exp 11/30/2025.
Lack of Assurance of Sterility
Apotex is recalling Ketorolac Tromethamine Ophthalmic Solution 0.5% 10mL eye drops because they may not be sterile. This could lead to eye infections if used. The recall applies to prescription-only products with specific batch and expiration details.
The product may not be sterile, which can lead to eye infections. This is a serious risk for people using the medication as prescribed.
Prescription users of Ketorolac eye drops with the specific NDC 60505-1003-2 and batch TZ1236. People with eye conditions requiring this medication are most at risk.
Check for the NDC code 60505-1003-2 and batch number TZ1236 on the label. The expiration date is November 30, 2025. This product is prescription-only.
Look for NDC 60505-1003-2 and batch TZ1236 on the label.
The recall states there is a lack of sterility assurance, so it may not be safe. Do not use until you confirm it's not recalled.
Check for NDC 60505-1003-2 and batch number TZ1236 on the label. The expiration date is November 30, 2025.
The recall does not specify a remedy, so contact Apotex for guidance.
We’ve drafted a message you can send Apotex to request your refund or repair — edit it as you like.
Subject: Recall D-0494-2025 — Apotex Apotex Hello, I own a Apotex that is covered by recall D-0494-2025 from Apotex. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
