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Drug FDA Class II Terminated Foreign material

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.

Evaric Pharmaceuticals Inc. Published Nov 27, 2024

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 55/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Evaric Pharmaceuticals Inc. or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Presence of Foreign Object: A pharmacist discovered a metal fragment embedded in a lisinopril 10 mg tablet.

Hazards

Metal Fragment · primary

Affected products (1)

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.

LISINOPRIL · 222, 600 bottles

NDC: 68645-608, 68645-609, 68645-610, 68645-611, 68645-612, 68645-613, 68645-609-90, 68645-610-90, 68645-611-90, 68645-608-90, 68645-612-90, 68645-613-90
Code info: Lot #: 241103, exp. date 05/31/2026

Affected areas

Nationwide

Timeline

  1. Initiated
    Nov 15, 2024
  2. Published
    Nov 27, 2024
  3. Terminated
    Apr 23, 2026
Recall number
D-0061-2025
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA drug enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.