MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF… — Class II medical device recall Z-2242-2016
Terminated recall by Encore Medical, Lp, reported 2016-07-27, distributed in CO, ID, TX. Reported failure of the instrument. The retaining ring component of a neck trial became disassembled from the
| Recall number | Z-2242-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Encore Medical, Lp, Austin, TX, United States |
| Recall initiated | 2016-06-21 |
| Classified | 2016-07-19 |
| Reported by FDA | 2016-07-27 |
| Terminated | 2017-01-10 |
| Distributed | CO, ID, TX |
| Lot numbers | 313R1000, 313R1900, 313R1901, 314R1000, 314R1900, 314R1901 |
| Model numbers | 200635, S-200636 |
Product
MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636
Reason for recall
Reported failure of the instrument. The retaining ring component of a neck trial became disassembled from the body of the neck.
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-2242-2016. 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.