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American Red Cross

Acme United Corporation · Model 720008 · UDI-DI 00092265720083

LRR

510(k) clearances

Adverse events

Recalls

146

Facilities

Description

Auto First Aid Zip Kit containing: BZK antiseptic towelettes (6); Conforming gauze roll, 2"; Fabric knuckle bandage; Fabric fingertip bandage; First aid cream packs, 0.9 gm each (2); First aid tape, 1/2" x 5 yd; Gauze dressing pads, 3" x 3" (2); Hand sanitizer packet; Insect relief pad; Moleskin pad, 2”x 2”; Nitrile gloves (4); Plastic adhesive bandages, 3/4" x 3" (5); Plastic patch bandage 1-1/2" x 1-1/2"; Red Cross First Aid Guide; Spot adhesive bandage, 7/8”’; Trauma pad, 5" x 9"; Sunscreen, SPF 30, 7 gm; Safety pins (2)

Recalls

Date	Firm	Reason
2026-03-27	North American Rescue LLC.	Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5 Error Code where the
2022-06-23	Family Dollar Stores, Llc.	Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
2022-04-05	Certified Safety Mfg Inc	First aid kit and cabinet components are being recalled by the supplier due to cGMP deviations at the manufacturer.
2022-03-11	Total Resources Intl	ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due
2022-03-11	Total Resources Intl	ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due
2022-03-02	ASO LLC	Kits contained recalled acetaminophen.
2020-06-05	HF Acquisition Co. LLC	A missing component (hand suction pump) in the emergency medical kits.
2020-06-04	HF Acquisition Co., LLC	Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
2020-06-04	HF Acquisition Co., LLC	Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
2020-06-04	HF Acquisition Co., LLC	Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.