FDA Device Intelligence
Home › Acme United Corporation › First Aid Only

First Aid Only

Acme United Corporation · Model 91055 · UDI-DI 00092265910552

LRR
10
510(k) clearances
25
Adverse events
30
Recalls
146
Facilities

Description

2 Person Emergency Preparedness Hurricane Backpack - Contains: Antiseptic Wipes 4 ct; Aspirin Tablets 2 ct; Biohazard Bags, 24" x 24", 10 Gallon Capacity, 4 ct; Cold Pack, 4" x 5; Crank Flashlight/Radio/Cell Phone Charger; Dotted Poly-Cotton Gloves; Duct Tape; Dust-Protection Face Mask 2 ct; Emergency Blanket, 52" x 84", 2 ct; Emergency Food Ba rs (6 pack), 2 ct; Emergency Water Packets, 4 oz., 12 ct; Emergency Water Pouch, 2.5 Gallons; Extra-Strength Non-Aspirin Tablets 2 ct; Fluoride Toothpaste Tube, 0.6 oz; Hand Warmers; Ibuprofen Tablets 2 ct; Light Stick, 2 ct; Multi-Tool; Alcohol Pads, 12 ct; Adhesive Bandages Plastic 0.75 X 3", 2 ct; Insect Sting Relief Pads, 4 ct; Junior Adhesive Bandages 0.38 x 1.5”, 10 ct; Triple Antibiotic Ointment Packet; Playing Cards; Poncho 2 ct: Sting Relief Wipes 2 ct; Toothbrush, 4", 2 ct; Tissues; Waterproof Matches; Whistle.

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.