PlainRecalls
FDA Drug Low Class III Terminated

DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-2829-1

Reported: March 15, 2023 Initiated: February 17, 2023 #D-0454-2023

Product Description

DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-2829-1

Reason for Recall

Labeling: Incorrect or Missing Lot and/or Exp Date

Details

Recalling Firm
Akron Pharma, Inc.
Units Affected
4,416 tubes
Distribution
Nationwide within the United States
Location
Fairfield, NJ

Frequently Asked Questions

What product was recalled?
DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-2829-1. Recalled by Akron Pharma, Inc.. Units affected: 4,416 tubes.
Why was this product recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date
Which agency issued this recall?
This recall was issued by the FDA Drug on March 15, 2023. Severity: Low. Recall number: D-0454-2023.