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Medi-First Standard Emergency Disaster Kit

Medique Products · Model 73911 · UDI-DI 00347682739119

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

Description

1 - Adhesive Bandage, 1” x 3” Strip, 16/box 1 - Adhesive Tape, Tri-Cut 5yd 1 - Alcalak Commissary Pack, 12x2/box 1 - Alcohol Prep Pads, 10/box 1 - Antiseptic Wipes, 10/box 1- APAP Commissary Pack, 12x2/box 1 - Burn Dressing 4” x 4” 1 - Cold Pack, Small, Boxed 1 - CPR Mask/Breathing Barrier 1 - Diamode Commissary Pack, 6x1/box 1 - Eyewash 4oz 1 - First Aid Handbook 1 - Flashlight, Hand Squeeze, Battery Free 1 - Food Ration 4 - Gauze Pad 3” x 3” 2 - Gauze Pad 4” x 4”, Sterile 1 - Gauze Roll 2” x 5yds 1 - Gauze Roll 3” x 5yds 2 - Glow Sticks 2 - Hand Warmers 1 - Matches, 50/box 1- Powder Free Exam Gloves, Disposable, Pair/L 1 - Rescue Blanket, 52” x 84” 1 - Scissors, EMT 7” 1 - Trauma Pad 5” x 9” 1 - Trauma Pad 10” x 30” 1 - Triangular Bandage with Pins, Non-Sterile 1 - Triple Antibiotic Ointment, 12/box 1 - Tweezers, Plastic, Disposable 4 - Water Pouch 1 - 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.

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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.