FDA recalls millions of prednisolone eye drops over potential contaminant risk
TL;DR Summary
The FDA issued a Class II recall of about 2.5 million bottles of prednisolone acetate ophthalmic suspension 1% eye drops by Lupin Pharmaceuticals due to a potential foreign-substance contamination. The products—available in 5 mL, 10 mL, and 15 mL sizes—were initially recalled on June 4 and reclassified on June 30; the drops treat non-infectious eye allergies and inflammation.
- Recall alert: 2.5M bottles of eye drops recalled for foreign substance Boston 25 News
- Millions of eye drops recalled nationwide. See affected products USA Today
- Millions of Eye Drop Bottles Recalled Over Contamination Concerns The New York Times
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- FDA recalls eye drops over possible 'foreign substance' upi.com
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