North American Rescue LLC. 2025-10-08 Health serious FDA
Health · FDA · Recall #FDA-Z-2637-2025
JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits: … Recall
Issued October 8, 2025 · North American Rescue LLC.
In October 2025, North American Rescue LLC. recalled the JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits: …, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT), REF: 30-0088, a component inside kits: … right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact North American Rescue LLC. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- North American Rescue LLC.
- Category
- Health
- Recall date
- October 8, 2025
- Units affected
- Not reported
- Sold at
- 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,
- Recall number
- FDA-Z-2637-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- North American Rescue LLC. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.