Sting Relief Swabs Recall: First Aid Only 19-001
Announced 2026-03-11 · FDA
The FDA recall involves Sting Relief Swabs, First Aid Only, 10 swabs per box (part number 19-001) distributed nationwide in the USA. The recall is due to a product mix-up and involves Lot 2251994, Exp 9/30/2029; 2,338 boxes are affected. No corrective action information is provided.
| Brand | ACME UNITED CORPORATION |
|---|---|
| Product | Sting Relief Swabs, First Aid Only, 10 Swabs per box, part number 19-001, Manufactured for: Acme United Corporation, 1 Waterview Dr. Shelton, CT, Made in the USA UPC 738743190015 |
| Reason | Product Mix-up |
| Severity | moderate |
| Units affected | 2338 boxes |
| Distribution | USA Nationwide |
| Agency | FDA |
| Recall / campaign no. | Lot #: 2251994, Exp 9/30/2029 |
WHAT YOU SHOULD DO
- Check your packaging for Lot number 2251994 and expiration date 9/30/2029 to determine if you are affected.
- If affected, do not use the product and contact the retailer or Acme United for return or replacement instructions.
- Keep the product and packaging until you receive instructions from the retailer or manufacturer.
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.