North American Rescue recalls

North American Rescue appears in 13 official U.S. recall notices indexed by RecallRadar, most recently on 2026-05-06.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

Recall summary

Recalls

• AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits designed for the ap…
  FDA Device · Class I · 2026-05-06 · North American Rescue
  Reason: 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 meter displays an E-5 error code for a…
• JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits: KIT, TCCC Training- Complete (Modules 1-3), REF: 85-0550
  FDA Device · Class II · 2025-10-08 · North American Rescue
  Reason: Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device and device performance during use.
• 10 ga ARS Decompression Needle, Part Number ZZ-0298
  FDA Device · Class II · 2021-09-29 · North American Rescue
  Reason: The device includes the incorrect Instructions for Use.
• 4 In. Flat Responder Emergency Trauma Dressing part number 30-0171, packaged in kits labeled as follows: a) M-FAK Mini First Aid Kit
  FDA Device · Class II · 2020-10-07 · North American Rescue
  Reason: Lack of sterility assurance of the 30-0171
• Range Trauma Kit - Product Code 85-1274, North American Rescue
  FDA Drug · Class II · 2016-12-14 · North American Rescue
  Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
• Advance Trauma Kit - Product Code 85-0742, 85-0746, 85-0745, 85-0639, 85-0744, 85-0744, 85-0741, North American Rescue
  FDA Drug · Class II · 2016-12-14 · North American Rescue
  Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
• Aid Backpack Kit - Product Code 85-0917, North American Rescue
  FDA Drug · Class II · 2016-12-14 · North American Rescue
  Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
• Range Trauma Kit ORG - Product Code 80-0213, 80-0299, 80-0298, North American Rescue
  FDA Drug · Class II · 2016-12-14 · North American Rescue
  Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
• Amphibious Trauma Kit - Product Code 85-0639, North American Rescue
  FDA Drug · Class II · 2016-12-14 · North American Rescue
  Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
• Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue
  FDA Drug · Class II · 2016-12-14 · North American Rescue
  Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
• Range Trauma Kit Hardcase - Product Code 85-0889, North American Rescue
  FDA Drug · Class II · 2016-12-14 · North American Rescue
  Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
• K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue
  FDA Drug · Class II · 2016-12-14 · North American Rescue
  Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
• USCG Boat Response Kit - Product Code 80-0353, North American Rescue
  FDA Drug · Class II · 2016-12-14 · North American Rescue
  Reason: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.