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Nearly 750K eye drops recalled. See affected products
USA Today • • business
Key Points:
- Sterling Pharmaceutical Services LLC has recalled 747,844 units of nine different eye drop products, including Walgreens-branded drops, due to concerns they may not be sterile, as reported by the FDA.
- The recall, initiated on August 20, 2026, and classified as Class II by the FDA on September 21, indicates the products could cause temporary or medically reversible health issues, with serious adverse effects considered unlikely.
- Affected products include various lubricant eye drops, a hypertonicity solution, and a nighttime ointment, with consumers advised to check product names, lot numbers, and expiration dates against the FDA recall list.
- Consumers who possess recalled products are urged to stop using them immediately and consult their healthcare providers for further advice.
- Sterling Pharmaceutical Services has not responded to requests for comment as of October 2, 2026.
