Ketorolac Tromethamine Recalls

2 recalls found for Ketorolac Tromethamine. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DRUG

Camber Ketorolac Tromethamine Injection Recall 2025 for Glass Particulates

Camber Pharmaceuticals recalled Ketorolac Tromethamine Injection, USP, 60 mg/2 mL, 2 mL single-dose vials distributed nationwide in the United States. The recall is due to the presence of glass particulates. Healthcare providers and patients should stop using the product immediately and contact Aspiro Pharma Limited at 1-866-495-1995 for guidance.

Ketorolac Tromethamine
Presence of
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Health & Personal Care
HIGH
FDA DRUG

Apotex Ketorolac Tromethamine Ophthalmic Solution Recall 2025: 493,468 Bottles Nationwide

Apotex Corp. is recalling 493,468 bottles of Ketorolac Tromethamine Ophthalmic Solution, 0.5%, Rx Only, sterile, distributed nationwide in the United States. The recall cites lack of assurance of sterility due to improper bottle sealing. Consumers and healthcare providers should stop using the product immediately and contact Apotex Corp. or their healthcare provider for guidance.

Apotex
Lack of
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Brand Statistics

Total Recalls
2
Pages
1

Related Brands

Camber PharmaceuticalsApotex