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Medi-First Large Vehicle Metal First Aid Kit

Medique Products · Model 807M1 · UDI-DI 00347682807016

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

Description

19818 - STD 1 EACH Mediwash eyewash 4oz 24402 – 1 EACH MF Antiseptic Spray 2oz Pump 22502 – 1 EACH MF Burn Spray Pump 2oz 221B - 0.002 M ALCOHOL PREP PADS-BULK 223B - 0.003 M MF TRIPLE ANTIBIOTIC .5gr BULK 60501 – 1 EACH 2" StrleConformGauze1s 60612 - STD 1 EACH 2"x2" Sterile Gauze Pad10s 60701 – 1 EACH Adhesive Tape 1/2 x5 yd 61450 – 1 EACH HW 7/8"X3" Woven Strip 50s 64101 - 1 EACH Bloodstopper Compress 9X5 (1s) 643B - 0.005 M HW Latex Free Woven Fingertip BULK 645B - 0.005 M HW Latex Free Woven Knuckle BULK 65001 - 1 EACH Tri cut Bandage non-sterile 1s + pins 75599 - 2 EACH Disposable Vinyl Gloves Pair/L 71401 - 1 EACH FIRST AID HANDBOOK 72401 – 1 EACH Ice Pack small/boxed EACH 77101 - 1 EACH WIRE SCISSORS 4.5" 77233 - 0.010 ECH Disposable Tweezers 100/bag 805B - STD 0.010 M MF/MFP ASPIRIN 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.