FDA Drug Recalls

Recalls / Class II

Class IID-0177-2017

Product

Range Trauma Kit - Product Code 85-1274, North American Rescue

Affected lot / code info
Kit Part # 85-1274 - Kit Lot # 85-1274072516W

Why it was recalled

Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.

Recalling firm

Firm
North American Rescue LLC.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
35 Tedwall Ct, N/A, Greer, South Carolina 29650-4791

Distribution

Quantity
unknown
Distribution pattern
Nationwide, Australia & Switzerland

Timeline

Recall initiated
2016-09-27
FDA classified
2016-12-08
Posted by FDA
2016-12-14
Terminated
2017-03-09
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0177-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.