FDA Medical Device Recalls (openFDA)
Zimmer Biomet Spine Inc.: 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
- Recall number
- Z-2318-2017
- Recalling firm
- Zimmer Biomet Spine Inc.
- 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
- Status
- Terminated
- Initiated
- 2017-05-10
- Posted
- 2017-05-15
- Terminated
- 2018-05-25
- Reason
- 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.
- Root cause
- Device Design
- Action
- Consignees will be notified on 5/15/17 via certified mail to return products.
- Quantity
- 497 units
- Distribution
- Nationwide, military/VA/govt and foreign consignee (No Canadian consignees)
- Lot, serial or model codes
- Model No: 07.02066.001 (All lots); 07.02053.001 (All lots distributed prior to April 26, 2017), and 730M0017 (Lot 309622)
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LYQ
- Firm FEI
- 3012447612
- Firm city
- Westminster
- Firm state
- CO
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28