Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
DIBUCAINE 1% HEMORRHOIDAL OINTMENT Recalled by Akron Pharma, Inc. Due to Labeling: Incorrect or Missing Lot and/or Exp Date
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Akron Pharma, Inc. directly.
Affected Products
DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-2829-1
Quantity: 4,416 tubes
Why Was This Recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Akron Pharma, Inc.
Akron Pharma, Inc. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report