Benzocaine Recall: Pearson Quality Topical Gel, Mint Flavor
FDA recall BNZ-001917 for Pearson Quality Topical Anesthetic Gel, Benzocaine 20%, Mint Flavor, 1 oz (30 g), manufactured for Pearson Dental Supply Inc. The recall is due to a defective container that may contain bottles with incomplete seals. Approximately 900 units were distributed nationwide in the USA; Exp 04/01/2029.
| Brand | Keystone Industries |
|---|---|
| Product | Pearson Quality Topical Anesthetic Gel (20% Benzocaine), Mint Flavor, Net Contents: 1 oz (3o g), Manufactured for: Pearson Dental Supply Inc., Sylmar, CA 91342 USA, NDC 43305-0009-3. |
| Reason | Defective container:may contain bottles with incomplete seals |
| Severity | moderate |
| Units affected | 150 |
| Distribution | Nationwide in the USA |
| Agency | FDA |
WHAT YOU SHOULD DO
- Stop using the recalled gel immediately.
- If you have the recalled product, do not use it and contact Pearson Dental Supply Inc. for instructions on return, refund, or disposal.
- Visit the FDA recall page or contact the manufacturer for more information on how to handle the recalled product.
How to identify the recalled item
| Lot / date codes | BNZ-001917, Exp 04/01/2029 |
|---|---|
| Lot / date codes | BNZ-001921, EXP 04/15/2029 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.