FDA-Device2016-07-27Class II
MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636
Encore Medical, Lp
Hazard
Reported failure of the instrument. The retaining ring component of a neck trial became disassembled from the body of the neck.
Sold states
CO, ID, TX
Affected count
14 (7 sets)
Manufactured in
9800 Metric Blvd, N/A, Austin, TX, United States
Products
MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2242-2016Don't want to check this manually?
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