ACME Sting Relief Swabs Recall: Product Mix-Up Hazard

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Recalling firmACME UNITED CORPORATION1 Waterview Dr Ste 200, N/A · Shelton, CT 06484-4368

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✎ GovInfoNow plain-language explainer

What happened, in plain English

ACME United is recalling Sting Relief Swabs (10 per box, part number 19-001) because of a product mix-up. This means the swabs might be the wrong product, which could lead to incorrect use or safety issues.

Why it’s dangerous

A product mix-up means the swabs could be the wrong product, leading to incorrect use. This might cause safety issues if the wrong swabs are used for first aid purposes.

Who’s affected

People who own or use Sting Relief Swabs with UPC 738743190015 and lot number 2251994 are affected. Those using the product for first aid purposes are most at risk due to potential mix-up.

How to tell if you have this one

Check for UPC 738743190015 and lot number 2251994 on the packaging. The product is labeled as 'Sting Relief Swabs, First Aid Only, 10 Swabs per box, part number 19-001'.

Brand
ACME UNITED
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for UPC 738743190015 and lot number 2251994 on the packaging to confirm if the product is affected.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The recall is for a product mix-up, meaning the swabs might be the wrong product, which could lead to incorrect use or safety issues.

What should I do if I have this product?

The recall notice does not specify a remedy, so check the product details to see if it matches the affected items.

Is there a deadline to take action?

The recall notice does not specify a deadline for action.

Take action

Contact ACME UNITED

We’ve drafted a message you can send ACME UNITED to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0122-2026 — ACME UNITED ACME UNITED

Hello,

I own a ACME UNITED that is covered by recall D-0122-2026 from ACME UNITED.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0122-2026 (September 23, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0122-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

ACME UNITED CORPORATION recalls Sting Relief Swabs, First Aid Only, 10 Swabs per box, part number 19-001, Manufactured for: Acme United Corporation, 1

Recall notice