DLC Laboratories, Inc: Drug Recall
Recall #D-0257-2021 · 01/06/2021
Class II: Risk
Recall Details
- Recall Number
- D-0257-2021
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- DLC Laboratories, Inc
- Status
- Terminated
- Date Initiated
- 01/06/2021
- Location
- Paramount, CA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 86,297 jars
Reason for Recall
Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product.
Product Description
Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar; Manufactured by/ Fabricado por: De La Cruz Products, A Division of DLC Laboratories, Inc. Paramount, CA 9023 USA; UPC 024286150426
Distribution Pattern
Distributed Nationwide and to the following foreign countries: Canada, Cambodia, Germany, and United Kingdom.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.