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Encore Medical, Lp recalls MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636
Recalled July 27, 2016 · FDA recall Z-2242-2016 · Encore Medical
Hazard
Reported failure of the instrument. The retaining ring component of a neck trial became disassembled from the body of the neck. · FDA Class II
Units
14 (7 sets)
Sold at
CO, ID, TX
Description
Reported failure of the instrument. The retaining ring component of a neck trial became disassembled from the body of the neck.
Product
MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636
Manufacturer(s)
Encore Medical, Lp
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →