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Medi-First Fanny Pack Basic Kit

Medique Products · Model 22473 · UDI-DI 00347682224738

LRR

510(k) clearances

Adverse events

Recalls

146

Facilities

Description

1 - Adhesive Bandage, 1” x 3” Strip, 16/box 2- Adhesive Bandage, 2” x 3” Patch 1 - Adhesive Tape, 1/2” x 5yd 1 - Ammonia Inhalants 6 - Antiseptic Wipes 2 - Burn Cream w/ Lidocaine, 0.9gm 1 - Cold Pack, Small 1 - CPR Mask/Breathing Barrier 1 - First Aid Handbook 3 - Gauze Pad 3” x 3” 5 - Insect Sting Relief Wipes 5 - Non-Aspirin Tablets, 2/pk 2 - Powder Free Exam Gloves, Disposable, Pair/L 1 - Scissors, 4.5” 1- Trauma Pad 5” x 9” 1 - Triangular Bandage with Pins, Non-Sterile 1 - Tweezers, Plastic, Disposable

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.