FDA Device Intelligence
HomeAcme United Corporation › First Aid Only

First Aid Only

Acme United Corporation · Model 1001-FAE-0103 · UDI-DI 00092265100113

LRR
10
510(k) clearances
13
Adverse events
30
Recalls
143
Facilities

Description

50 Person Large Plastic SmartCompliance First Aid Kit - Contains: Adhesive Fabric Bandages, 1" x 3", 25 ct; Adhesive Plastic Bandages, 0.75" x 3", 25 ct; Alcohol Pads, 20 ct: Antibiotic Ointment Packets, 10 ct; Antiseptic Wipes, 20 ct; Butterfly Wound Closures, 10 ct; Castile Soap Towelettes, 10 ct; Conforming Gauze Roll, 2"; Conforming Gauze Roll, 3"; CPR Face Shield and 2 Nitrile Exam Gloves; Elastic Bandage Wrap, 2" x 5 yd; Fingertip Fabric Bandages, 10 ct; First Aid Guide; First Aid Tape, 1/2" x 10 yd; First Aid/Burn Cream Packets, 10 ct; Knuckle Fabric Bandages, 10 ct; Moleskin Blister Prevention, 2" x 2", 10 ct; Nitrile Exam Gloves, 4 ct; Patch Plastic Bandages, 1.5" x 1.5", 10 ct; Scissors; Sterile Gauze Pads, 2" x 2", 10 ct; Sterile Gauze Pads, 3" x 3", 10 ct; Trauma Pad, 5" x 9; Triangular Bandage, 40" x 40" x 56"; Tweezers.

Recalls

DateFirmReason
2026-03-27North 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
2022-06-23Family Dollar Stores, Llc.Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
2022-04-05Certified Safety Mfg IncFirst aid kit and cabinet components are being recalled by the supplier due to cGMP deviations at the manufacturer.
2022-03-11Total Resources IntlULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due
2022-03-11Total Resources IntlULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due
2022-03-02ASO LLCKits contained recalled acetaminophen.
2020-06-05HF Acquisition Co. LLCA missing component (hand suction pump) in the emergency medical kits.
2020-06-04HF Acquisition Co., LLCInstead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
2020-06-04HF Acquisition Co., LLCInstead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
2020-06-04HF Acquisition Co., LLCInstead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.