Recalls / Class II
Class IID-0061-2025
Product
Lisinopril Tablets, USP 10 mg, 90 tablets per bottle, Rx Only, Distributed by: Walmart, Bentonville, AR 72716, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045, NDC# 68645-610-90.
- Brand name
- Lisinopril
- Generic name
- Lisinopril
- Active ingredient
- Lisinopril
- Route
- Oral
- NDCs
- 68645-608, 68645-609, 68645-610, 68645-611, 68645-612, 68645-613
- FDA application
- ANDA075903
- Affected lot / code info
- Lot #: 241103, exp. date 05/31/2026
Why it was recalled
Presence of Foreign Object: A pharmacist discovered a metal fragment embedded in a lisinopril 10 mg tablet.
Recalling firm
- Firm
- Evaric Pharmaceuticals Inc.
- Manufacturer
- Legacy Pharmaceutical Packaging, LLC
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 155 Commerce Dr, N/A, Hauppauge, New York 11788-3925
Distribution
- Quantity
- 222, 600 bottles
- Distribution pattern
- Nationwide in the USA
Timeline
- Recall initiated
- 2024-11-15
- FDA classified
- 2024-11-20
- Posted by FDA
- 2024-11-27
- Status
- Completed
Source: openFDA Drug Enforcement endpoint. Recall record D-0061-2025. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.