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Synthes (USA) Products LLC recalls Synthes Application Instrument for Sternal ZIPFIX; indications for use include primary or secondary closure/repair of th
Recalled September 2, 2015 · FDA recall Z-2475-2015 · Synthes (USA) Products
Hazard
The end cap may loosen and detach making the instrument non-functional. No injuries reported. · FDA Class II
Units
451
Sold at
Nationwide and internationally to Canada.
Description
The end cap may loosen and detach making the instrument non-functional. No injuries reported.
Product
Synthes Application Instrument for Sternal ZIPFIX; indications for use include primary or secondary closure/repair of the sternum following sternotomy or fracture of the sternum to stabilize the sternum and promote fusion
Manufacturer(s)
Synthes (USA) Products LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →