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Medtronic Navigation, Inc. recalls DISP 9730950 STRL SPHERE, 1 PK INSERT
Recalled November 26, 2014 · FDA recall Z-1581-2014 · Medtronic Navigation
Hazard
Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility. · FDA Class II
Units
26,674 total
Sold at
Nationwide Distribution
Description
Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.
Product
DISP 9730950 STRL SPHERE, 1 PK INSERT
Manufacturer(s)
Medtronic Navigation, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →