DermaMed Ointment 2% Recall: CGMP Deviations
DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt. 106 g (3.75 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue…
What is the FDA recall status?
The FDA record lists this recall as ongoing. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions and check the agency notice or firm for current guidance.
Why was DermaMed Ointment 2% recalled?
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
What should I do if I have this product?
Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare your product with the product description and available lot, UPC or model codes below from the official FDA record to check whether it is covered by this recall. If an identifier is missing or unclear, check the complete official notice or contact the firm; an incomplete match here does not establish that your product is unaffected.
Full product description
DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt. 106 g (3.75 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-214-04
Which lot codes, UPCs or models are affected?
All lots on or before expiry date 08/2027
- Agency record number
- D-0164-2026
- Product
- DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt. 106 g (3.75 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue…
- Recalling firm
- DermaRite Industries, LLC
- Quantity
- 2,673 tubes
- Distribution
- Nationwide in the USA
- Recall started
- August 27, 2025
- Report date
- November 26, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (drug)