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North American Rescue Recalls
13 recalls on record · December 14, 2016 to May 6, 2026 · Drugs, Medical Devices
Recalls by year
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26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 6, 2026Medical DevicesFDA
North American Rescue LLC. recalls AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits
Hazard: 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 very high blood glucose event (> 600 mg/dL) or when there is a test strip error, which can lead to operator confusion when evaluating patients and a delay in appropriate treatment. This is a downstream recall of Trividia Health Class I, Recall Event ID 98317.
October 8, 2025Medical DevicesFDA
North American Rescue LLC. recalls JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits: KIT, TCCC Training- Complete (Mod
Hazard: 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.
September 29, 2021Medical DevicesFDA
North American Rescue LLC. recalls 10 ga ARS Decompression Needle, Part Number ZZ-0298
Hazard: The device includes the incorrect Instructions for Use.
October 7, 2020Medical DevicesFDA
North American Rescue LLC. recalls 4 In. Flat Responder Emergency Trauma Dressing part number 30-0171, packaged in kits labeled as follows: a) M-FAK Min
Hazard: Lack of sterility assurance of the 30-0171
December 14, 2016DrugsFDA
North American Rescue LLC. recalls USCG Boat Response Kit - Product Code 80-0353, North American Rescue
Hazard: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
December 14, 2016DrugsFDA
North American Rescue LLC. recalls Aid Backpack Kit - Product Code 85-0917, North American Rescue
Hazard: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
December 14, 2016DrugsFDA
North American Rescue LLC. recalls Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue
Hazard: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
December 14, 2016DrugsFDA
North American Rescue LLC. recalls Amphibious Trauma Kit - Product Code 85-0639, North American Rescue
Hazard: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
December 14, 2016DrugsFDA
North American Rescue LLC. recalls K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue
Hazard: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
December 14, 2016DrugsFDA
North American Rescue LLC. recalls Advance Trauma Kit - Product Code 85-0742, 85-0746, 85-0745, 85-0639, 85-0744, 85-0744, 85-0741, North American Rescue
Hazard: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
December 14, 2016DrugsFDA
North American Rescue LLC. recalls Range Trauma Kit - Product Code 85-1274, North American Rescue
Hazard: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
December 14, 2016DrugsFDA
North American Rescue LLC. recalls Range Trauma Kit ORG - Product Code 80-0213, 80-0299, 80-0298, North American Rescue
Hazard: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
December 14, 2016DrugsFDA
North American Rescue LLC. recalls Range Trauma Kit Hardcase - Product Code 85-0889, North American Rescue
Hazard: Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.