Class III
Ongoing
Xelpros (latanoprost ophthalmic emulsion) 0.005%, 125mcg/2.5mL, 2.5 mL bottle, Rx only, Manufactured by: Sun Pharmaceutical Ind. Ltd., India., NDC 47335-317-90
This recall is currently active, issued May 29, 2024. It was issued by Sun Pharmaceutical Industries Inc.
- Recall Initiated
- April 22, 2024
- Posted
- May 29, 2024
- Recall Number
- D-0502-2024
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 35,069 bottles
- Firm Location
- Princeton, NJ, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Failed Release Testing: Out of specification for particulate matter test.
Distribution
TX, PA
Lot / Code Info
Lot #: HAD3383A, Exp 8/31/2024
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