Vitality Spinal Fixation System — Class II medical device recall Z-2318-2017
Terminated recall by Zimmer Biomet Spine Inc., reported 2017-06-14, distributed nationwide. Zimmer Biomet is conducting a medical device recall for Vitality T27 Final Drivers and Vitality Torque Limitin
| Recall number | Z-2318-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet Spine Inc., Westminster, CO, United States |
| Recall initiated | 2017-05-10 |
| Classified | 2017-06-08 |
| Reported by FDA | 2017-06-14 |
| Terminated | 2018-05-25 |
| Distributed | Nationwide (US) |
| Quantity | 497 units |
| Reason classes | specification failure |
| Lot numbers | 07.02053.001, 309622 |
| Model numbers | 07.02053.001, 07.02066.001, 730M0017 |
Product
Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs Model Number(s): 07.02066.001, 07.02053.001, 730M0017
Reason for recall
Zimmer Biomet is conducting a medical device recall for Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs because when applying torque to tighten the closure top the driver has the potential to create a torsional spring which can cause damage and the potential for the values of torque to go out of specification.
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-2318-2017. 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.