FDA Recall D-0122-2026
ACME UNITED CORPORATION · Shelton, CT
Class II Ongoing 233 days on record
Moderate impact — Class II recall — temporary or medically reversible adverse health consequence possible; remote probability of serious adverse health consequence.
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 for recall
Product Mix-up
Recall record
- Recall number
D-0122-2026- Classification
- Class II
- Status
- Ongoing
- Voluntary or mandated
- Voluntary: Firm initiated
- Firm notification
- N/A
- Distribution
- USA Nationwide
- Recall initiated
- 2025-09-23
- Classified by FDA Center
- 2025-10-28
- FDA published
- 2025-11-05
- Recalling firm
- ACME UNITED CORPORATION
- Firm location
- Shelton, CT
Operational response
Class II recalls indicate possible temporary or reversible health consequences. Remove affected lots from active dispensing. Segregate inventory. Check the firm’s recall notification for guidance on patient outreach.
For the official FDA enforcement record, see FDA's Recall Search.