FDA Device recall Z-2242-2016
MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636
- FDA Device
- Class II
- terminated
- Published 2016-07-27
On 2016-07-27 the FDA classified a Class II recall of MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636 by Encore Medical, citing reported failure of the instrument. The retaining ring component of a neck trial became disassembled from the body of the neck.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2242-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-06-21 |
| Published | 2016-07-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Encore Medical |
| Distribution | CO, ID, TX |
Product
MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636
Reason
Reported failure of the instrument. The retaining ring component of a neck trial became disassembled from the body of the neck.
Identifiers
| code_info | Lot: 313R1000, 313R1900, 313R1901, 314R1000, 314R1900, 314R1901 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2242-2016%22
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