SUN PHARMACEUTICAL INDUSTRIES INC 2024-05-29 Health moderate FDA
Health · FDA · Recall #FDA-D-0502-2024
Xelpros (latanoprost ophthalmic emulsion) 0.005%, 125mcg/2.5mL, 2.5 mL bottle, Rx only,… Recall
Issued May 29, 2024 · SUN PHARMACEUTICAL INDUSTRIES INC
In May 2024, SUN PHARMACEUTICAL INDUSTRIES INC recalled the Xelpros (latanoprost ophthalmic emulsion) 0.005%, 125mcg/2.5mL, 2.5 mL bottle, Rx only,…, a moderate health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Failed Release Testing: Out of specification for particulate matter test.
What you should do
- 1 Stop using Xelpros (latanoprost ophthalmic emulsion) 0.005%, 125mcg/2.5mL, 2.5 mL bottle, Rx only,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact SUN PHARMACEUTICAL INDUSTRIES INC to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- SUN PHARMACEUTICAL INDUSTRIES INC
- Category
- Health
- Recall date
- May 29, 2024
- Units affected
- Not reported
- Sold at
- TX, PA
- Recall number
- FDA-D-0502-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- SUN PHARMACEUTICAL INDUSTRIES INC has 34 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.