Greer, SC, United States
North American Rescue LLC. recalls
4 recalls recorded since 2018, most recently on 27 March 2026. 2 are listed as ongoing. Status and classification are as published by the FDA.
Recalls4
Ongoing (FDA)2
Terminated or completed2
Class I (FDA)1
Ongoing Class I Medical devices
- Recall started
- 27 March 2026
- 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 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.
- Distribution
- US: CA, WA
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1947-2026
- 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 /
Ongoing Class II Medical devices
- Recall started
- 1 July 2025
- 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.
- Distribution
- Worldwide - US Nationwide distribution in the states of SC, OK, ID, KY, VA, NV, IL, TX, CA, FL, LA, NY, LA, ME, PA, AR, AZ, AL, DE, MA, MS, HI, WA, MI, GA, NJ, UT, MD, OR, NC, NC, AL and the countries of KOR, JPN, BWA, SAU, BEL.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2637-2025
- 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 EXPEDITIO
Terminated Class II Medical devices
- Recall started
- 27 August 2021
- Terminated
- 19 January 2024
- Reason
- The device includes the incorrect Instructions for Use.
- Distribution
- Distribution throughout US and Puerto Rico OUS consignees in Australia, Czech Republic, Denmark, France, Germany, Ireland, Italy, Poland, and Switzerland
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2520-2021
- 10 ga ARS Decompression Needle, Part Number ZZ-0298
Terminated Class II Medical devices
- Recall started
- 21 August 2020
- Terminated
- 31 January 2024
- Reason
- Lack of sterility assurance of the 30-0171
- Distribution
- US Nationwide distribution
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-3018-2020
- 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 Dre
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.