Akron Pharma, Inc. recalls DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-282
Recalled March 15, 2023 · FDA recall D-0454-2023 · Akron Pharma
Hazard
Labeling: Incorrect or Missing Lot and/or Exp Date · FDA Class III
Units
4,416 tubes
Sold at
Nationwide within the United States
Description
Labeling: Incorrect or Missing Lot and/or Exp Date
Product
DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-2829-1
Manufacturer(s)
Akron Pharma, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →