FDA Device Intelligence
Home › Medique Products › Medi-First Interational Traveler First Aid Kit

Medi-First Interational Traveler First Aid Kit

Medique Products · Model 77501 · UDI-DI 00347682775018

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

Description

6 Adhesive Bandage, 7/8” x 3” Strip 2 Adhesive Bandage, 2” x 3” Patch 2 Adhesive Bandage, Knuckle 1 Adhesive Tape 1/2” x 2.5yds 8 Alcalak Tablets, 2pk 6 Antiseptic Towelettes 8 APAP XS Tablets, 2pk 4 Butterfly Bandage, Large 8 CCP Caffeine Free Tablets, 2pk 4 Chlorphen Tablets, 2pk 8 Diamode Tablets, 1pk 12 Decorel Forte Plus, 2pk 16 Diotame Tablets, 2pk 1 Elastic Wrap w/ Clips 2” 1 Elastic Wrap w/ Clips 4” 1 Eye Wash, 1oz 4 Gauze Pad 4” x 4”, Sterile 1 Gauze Roll 3” x 5yds 2 Hydrocortisone Cream, 1gm 2 Insect Sting Relief Wipes 2 Iodine Swabs 8 I-Prin Tablets, 2pk 6 Medikoff Drops 1 Powder Free Exam Gloves, Disposable, Pair/L 2 Thermometer, Disposable Forehead 1 Traveler Advice Card 1 Triangular Bandage with Pins, Non-Sterile 2 Triple Antibiotic Ointment, .5g 2 Safety Pins 1 Scissors,

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.