Stryker AVS Navigator Trials 6mm-15mm Manufactured by: Stryker Spine… — Class II medical device recall Z-2033-2012
Terminated recall by Stryker Spine, reported 2012-07-25, distributed nationwide. Beginning in February 2011, Stryker Spine began receiving reports related to the shaft of the AVS Navigator tr
| Recall number | Z-2033-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Spine, Allendale, NJ, United States |
| Recall initiated | 2012-01-13 |
| Classified | 2012-07-19 |
| Reported by FDA | 2012-07-25 |
| Terminated | 2013-07-29 |
| Distributed | Nationwide (US) |
| Quantity | 273 units |
| Lot numbers | 104864, 104866, 104867, 104868, 104869, 104870, 104871, 104872, 104873, 104874, 104875, 10E331 |
| Model numbers | 48392206, 48392207, 48392208, 48392209, 48392210, 48392211, 48392212, 48392213, 48392214, 48392215 |
Product
Stryker AVS Navigator Trials 6mm-15mm Manufactured by: Stryker Spine SAS Z.1 Marticot-33610-Cestas -France +33 (0) 5.57.97.06.30 http;//www.stryker.com Distributed in the USA by Stryker Spine 2 Pearl Court. Allendale NJ 07401-1677 USA +1-201-780-8000 Cestas France 33610. Intended Use: The trials are designed and intended to measure the height of the disc space intra-operatively.
Reason for recall
Beginning in February 2011, Stryker Spine began receiving reports related to the shaft of the AVS Navigator trial failing at the junction of the trial head.
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-2033-2012. 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.