Sting Relief Swabs, First Aid Only, 10 Swabs per box, part number 19-001, Manufactured for: Acme United Corporation, 1 W
Summary
The FDA issued a Class II for Sting Relief Swabs, First Aid Only, 10 Swabs per box, part number 19-001, Manufa by ACME UNITED CORPORATION. Reason: Product Mix-up.
Details
Source
Drug Recall
External ID
D-0122-2026
Action Date
2025-11-05
Status
Ongoing
Category
drug
Product Description
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
Lot/Code Info: Lot #: 2251994, Exp 9/30/2029
Quantity Affected: 2338 boxes
Reason for Recall
Product Mix-up
Distribution
USA Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-23
Company
Shelton, CT
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 95 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
ACME UNITED CORPORATION has 22 FDA actions in our database, including 22 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (ACME UNITED CORPORATION) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ACME UNITED CORPORATION have FDA actions?
ACME UNITED CORPORATION has 22 FDA actions in our database, including 22 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0122-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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