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Adventurer Kit

Altitude Technologies Inc. · Model 01424RD · UDI-DI 00850018201407

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

Description

This emergency first aid kit is packed full of necessary first aid supplies to treat a variety of issues to include dehydration, scrapes, cuts, and over-the-counter medications for multiple ailments. The Adventurer Kit also includes an emergency survival blanket, elastic bandage wrap, and an irrigation syringe to prepare you for your next exciting adventure!

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.