FDA Drugs recall ·
Furosemide Tablets, USP 40 mg, 1,000 Tablets, Rx Only… recall
- Recall number
- D-0293-2026
- Date
- (initiated January 10, 2026)
- Company / brand
- Graviti Pharmaceuticals Private Limited
E & 621 Patancheru Mandal, Hyderabad, India - Category
- Drugs › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 4212 bottles
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Furosemide Tablets, USP 40 mg, 1,000 Tablets, Rx Only, Manufactured for: Rising Pharmaceuticals Inc., East Brunswick, NJ 08816, Manufactured by: Graviti Pharmaceuticals Pvt. Ltd. Telangana - 502307, India, NDC 64980-563-10.
Why was it recalled?
Presence of Foreign Substance
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot# FUB125042G; Exp. 05/13/2027
Distribution
U.S. Nationwide
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (drugs), recall D-0293-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.