FDA Device Intelligence
HomeAdventure Ready Brands › Adventure Medical Kits

Adventure Medical Kits

Adventure Ready Brands · Model 1 · UDI-DI 00707708102103

LRR
10
510(k) clearances
12
Adverse events
30
Recalls
143
Facilities

Description

Adventure First Aid, 1.0 Bandage Materials 12 - Bandage, Adhesive, Fabric, 1" x 3" 1 - Bandage, Adhesive, Fabric, 2" x 4.5" 2 - Bandage, Adhesive, Fabric, Knuckle 3 - Bandage, Butterfly Closure 2 - Dressing, Gauze, Sterile, 2" x 2", Pkg./2 2 - Dressing, Gauze, Sterile, 3" x 3", Pkg./2 Blister / Burn 1 - Moleskin, 3" x 4" Fracture / Sprain 1 - Bandage, Elastic with Clips, 2" Instrument 1 - Splinter Picker/Tick Remover Forceps Medication 2 - Acetaminophen (500 mg), Pkg./2 2 - After Bite Wipe 2 - Antihistamine (Diphenhydramine 25 mg) 1 - Aspirin (325 mg), Pkg./2 2 - Ibuprofen (200 mg), Pkg./2 Survival Tools 1 - Compass, Button, Liquid Filled 1 - Mini Rescue Howler Whistle Wound Care 10 - Antiseptic Wipe 1 - Tape, 1/2" x 10 Yards 2 - Triple Antibiotic Ointment, Single Use

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.