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All product recalls associated with North American Rescue LLC..
Total Recalls
12
Past Year
1
Class I (Serious)
0
Most Recent
Jul 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
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.
The device includes the incorrect Instructions for Use.
Lack of sterility assurance of the 30-0171