Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 Recalled by Encore Medical, Lp Due to Reported failure of the instrument. The retaining ring...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Encore Medical, Lp directly.
Affected Products
MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636
Quantity: 14 (7 sets)
Why Was This Recalled?
Reported failure of the instrument. The retaining ring component of a neck trial became disassembled from the body of the neck.
Where Was This Sold?
This product was distributed to 3 states: CO, ID, TX
About Encore Medical, Lp
Encore Medical, Lp has 43 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report