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First Aid Only

Acme United Corporation · Model 06090 · UDI-DI 00738743060905

LRR

510(k) clearances

Adverse events

Recalls

146

Facilities

Description

25 Person Basic First Aid Kit - Contains: Adhesive Bandage, Plastic 1 X 3", 8 ct; Adhesive Tape 1/2"x 5 yd; Antiseptic wipes, 10 ct; Cold Pack 4 x 5"; Combine Dressing 5"x 9"; Dressing, NonStick Pad with Adhesive Tabs; First Aid Burn Cream Packets, 6 ct; Nitrile Exam Gloves, 2 ct; Red Cross First Aid Guide; Sterile Gauze Pads, 3"x 3", 2 ct; Triangular Bandage; Triple Antibiotic Packets, 6 ct.

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.