djosurgical Linear Neck Trials with Spring Sides — Class II medical device recall Z-1692-2020
Ongoing recall by Encore Medical, LP, reported 2020-04-22, distributed in CA, CO, MD, MN, OH, TX, WA. The retaining ring on the neck trials has a potential to fail interoperatively.
| Recall number | Z-1692-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Encore Medical, LP, Austin, TX, United States |
| Recall initiated | 2018-07-10 |
| Classified | 2020-04-10 |
| Reported by FDA | 2020-04-22 |
| Distributed | CA, CO, MD, MN, OH, TX, WA |
| Model numbers | 2000635, 200635, 200636, 313R1000, 313R1900, 313R1901, 314R1000, 314R1900, 314R1901 |
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 for recall
The retaining ring on the neck trials has a potential to fail interoperatively.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1692-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.