Lupin Pharmaceuticals Inc. 2026-07-08 Health serious FDA
Health · FDA · Recall #FDA-D-0655-2026
prednisoLONE Acetate Ophthalmic Suspension, USP, 1%, Rx only, Sterile, a) 5 mL (NDC… Recall
Issued July 8, 2026 · Lupin Pharmaceuticals Inc.
In July 2026, Lupin Pharmaceuticals Inc. recalled the prednisoLONE Acetate Ophthalmic Suspension, USP, 1%, Rx only, Sterile, a) 5 mL (NDC…, a serious 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 Dana Whitfield, RecallCheckr
What this means for you
Presence of Foreign Substance
What you should do
- 1 Stop using prednisoLONE Acetate Ophthalmic Suspension, USP, 1%, Rx only, Sterile, a) 5 mL (NDC… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Lupin Pharmaceuticals 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
- Lupin Pharmaceuticals Inc.
- Category
- Health
- Recall date
- July 8, 2026
- Units affected
- Not reported
- Sold at
- U.S. Nationwide
- Recall number
- FDA-D-0655-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Lupin Pharmaceuticals Inc. has 21 recalls in our database, including 1 rated Critical.
- We're tracking 3,673 Health recalls in our database.
- This is the 453rd Health recall we've logged in 2026.