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Medi-First 36 Unit Metal First Aid Kit

Medique Products · Model 36UMA · UDI-DI 00347682368623

LRR
10
510(k) clearances
13
Adverse events
30
Recalls
146
Facilities

Description

6771B - 2 EACH 4" Compress 61270 - 3 EACH 3"X3" Sterile Gauze Pads 4 63775 – 2 EACH 3/4"x3" Plastic Strip 16 68999 – 1 EACH 2" Stretch Roller Gauze Unit 62612 – 1 EACH Fingertip Woven M/L 10s 60075 – 4 EACH 1"X3" Plastic Strip 16s 62730 – 1 EACH Woven Knuckle 8s 6501B – 2 EACH Triangular Band W/Pins 40" 73699 – 1 EACH Disposable Nitrile Gloves 2s Unit 22612 – 1 EACH Ammonia Wipes (10) 22312 – 2 EACH Triple Antibiotic Ointment 10c 21412 - STD 2 EACH Antiseptic Towelettes 5X7 10s 22112 – 2 EACH Alcohol Prep Pads 10s 72401 – 1 EACH Ice Pack small/boxed 77901 - STD 1 EACH Eye Unit (eyewash, tape, pad) 47769 - STD 2 EACH Burn Gel w/Lido 6s 65699 – 3 EACH 1/2"X2.5yd Adhesive Tape 2s 7371B - 1. EACH Forceps and Scissor Unit 3060 - 1 EACH BurnAid Dress4x4 + 80201 - 1 EACH CPR Mask 89801 – 2 EACH ABD Sterile 5x9 1s 17378 - 0.006 M Hand Sanitizer Bulk

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.

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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.