FDA Device recall Z-1692-2020
djosurgical Linear Neck Trials with Spring Sides, Standard, nonsterile, REF S-200635
- FDA Device
- Class II
- ongoing
- Published 2020-04-22
On 2020-04-22 the FDA classified a Class II recall of djosurgical Linear Neck Trials with Spring Sides, Standard, nonsterile, REF S-200635 by Encore Medical, citing the retaining ring on the neck trials has a potential to fail interoperatively.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1692-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2018-07-10 |
| Published | 2020-04-22 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Encore Medical |
| Distribution | CA, CO, MD, MN, OH, TX, WA |
Product
djosurgical Linear Neck Trials with Spring Sides, Standard, nonsterile, REF S-200635; and djosurgical Linear Neck Trials with Spring Sides, Lateral, nonsterile, REF S-200636. The firm name on the label is djosurgical, Austin, TX.
Reason
The retaining ring on the neck trials has a potential to fail interoperatively.
Identifiers
| code_info | All Revision C trials. REF S-2000635: 313R1000, 313R1900, 313R1901; REF S-200636: 314R1000, 314R1900, 314R1901. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1692-2020%22
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