Tolmar, Inc. 2022-08-10 Health serious FDA
Health · FDA · Recall #FDA-D-1300-2022
Naftifine Hydrochloride Gel, USP 1%, packaged in cartons with: a) Net Wt. 90g tube (NDC… Recall
Issued August 10, 2022 · Tolmar, Inc.
In August 2022, Tolmar, Inc. recalled the Naftifine Hydrochloride Gel, USP 1%, packaged in cartons with: a) Net Wt. 90g tube (NDC…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Failed Impurities/ degradation specifications: Out-of-Specification test results obtained for Unspecified Impurity Relative Retention Time
What you should do
- 1 Stop using Naftifine Hydrochloride Gel, USP 1%, packaged in cartons with: a) Net Wt. 90g tube (NDC… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Tolmar, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Tolmar, Inc.
- Category
- Health
- Recall date
- August 10, 2022
- Units affected
- Not reported
- Sold at
- distributed to 1 consignee in KY.
- Recall number
- FDA-D-1300-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Tolmar, Inc. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.