Manufacturer

North American Rescue LLC.

13 recalls in our database name North American Rescue LLC. as the manufacturing or recalling firm.

What the numbers show

Total: 13
Critical: 0
Severe: 9
Most recent: 2026-05-06

Of the 13 recalls from North American Rescue LLC. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 9 (69%) are Severe.

Which agencies issued them

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–13 of 13

SevereFDA (Devices)·Z-1947-2026·2026-05-06
AIDBAG First Aid Kits with Recalled Blood Glucose Meters Recalled
North American Rescue LLC. is recalling AIDBAG first aid kits containing McKesson TRUE Metrix PRO blood glucose meters that display an E-5 error code incorrectly, potentially delaying appropriate patient treatment.
Product
AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits designed for the appropriate level provider to evaluate and treat patients at the point-of-injury / point-of-illness. The original manufacturer labeling, includ
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-2637-2025·2025-10-08
Junctional tourniquet devices recalled over manufacturing defect affecting structural integrity
North American Rescue is recalling 552 Junctional Emergency Treatment Tools over a potential manufacturing defect that may compromise structural integrity and performance during use.
Product
JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits: KIT, TCCC Training- Complete (Modules 1-3), REF: 85-0550; KIT, TCCC MODULE ONE - SKILLS, REF: 85-0519; KIT, MULTI MISSION EXPEDITIONARY RESPONSE - MMERK, REF: 85-2420; KIT, TCCC SKILLS/IFAK
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2520-2021·2021-09-29
Decompression Needle Recall Due to Incorrect Instructions for Use
North American Rescue is recalling 51,424 units of 10 ga ARS Decompression Needles due to incorrect Instructions for Use. Affected parties should stop using and contact manufacturer.
Product
10 ga ARS Decompression Needle, Part Number ZZ-0298
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-3018-2020·2020-10-07
North American Rescue Recalls Emergency Trauma Dressings Due to Sterility Concerns
North American Rescue LLC is recalling 4 In. Flat Responder Emergency Trauma Dressings because they may lack sterility assurance. The affected dressings are packaged in various first aid and trauma kits.
Product
4 In. Flat Responder Emergency Trauma Dressing part number 30-0171, packaged in kits labeled as follows: a) M-FAK Mini First Aid Kit; Kit Product Code: 80-0890 b) M-FAK Mini First Aid Kit, with Bleeding Control Dressing; Kit Product Code: 80-0891 c) M-FAK Mini First Aid
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0181-2017·2016-12-14
North American Rescue Recalls Mini Resupply Trauma Kits Due to Sterility Concerns
North American Rescue LLC is recalling Mini Resupply Trauma Kits because the manufacturer has concerns about the sterility of the included eye wash solution.
Product
Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0177-2017·2016-12-14
North American Rescue Recalls Range Trauma Kits Due to Sterility Concerns
North American Rescue LLC is recalling Range Trauma Kits because the manufacturer has concerns about the sterility of the eye wash solution.
Product
Range Trauma Kit - Product Code 85-1274, North American Rescue
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0175-2017·2016-12-14
North American Rescue Recalls Range Trauma Kits Due to Sterility Concerns
North American Rescue LLC is recalling Range Trauma Kit Hardcases because the manufacturer has concerns about the sterility of the eye wash irrigating solution included in the kits.
Product
Range Trauma Kit Hardcase - Product Code 85-0889, North American Rescue
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0180-2017·2016-12-14
North American Rescue Recalls Amphibious Trauma Kits Due to Sterility Concerns
North American Rescue is recalling Amphibious Trauma Kits because the manufacturer has concerns about the sterility of the eye wash solution.
Product
Amphibious Trauma Kit - Product Code 85-0639, North American Rescue
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0183-2017·2016-12-14
North American Rescue Recalls USCG Boat Response Kits Due to Sterility Concerns
North American Rescue LLC is recalling USCG Boat Response Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.
Product
USCG Boat Response Kit - Product Code 80-0353, North American Rescue
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0182-2017·2016-12-14
North American Rescue Recalls Aid Backpack Kits Due to Sterility Concerns
North American Rescue LLC is recalling Aid Backpack Kits because the manufacturer has concerns about the sterility of the eye wash irrigating solution.
Product
Aid Backpack Kit - Product Code 85-0917, North American Rescue
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0178-2017·2016-12-14
North American Rescue Recalls Advance Trauma Kits Due to Sterility Concerns
North American Rescue LLC is recalling Advance Trauma Kits because the manufacturer has concerns regarding the sterility of the eye wash irrigating solution.
Product
Advance Trauma Kit - Product Code 85-0742, 85-0746, 85-0745, 85-0639, 85-0744, 85-0744, 85-0741, North American Rescue
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0179-2017·2016-12-14
North American Rescue Recalls K-9 Trauma Field Kits Due to Sterility Concerns
North American Rescue LLC is recalling K-9 Trauma Field Kits because the manufacturer has concerns about the sterility of the included eye wash irrigating solution.
Product
K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0176-2017·2016-12-14
North American Rescue Recalls Range Trauma Kits Due to Sterility Concerns
North American Rescue is recalling specific Range Trauma Kits because the manufacturer has concerns about the sterility of the included eye wash solution.
Product
Range Trauma Kit ORG - Product Code 80-0213, 80-0299, 80-0298, North American Rescue
Category
Medical Device
Distribution
Distributed nationwide