Trinica Bone Tap Instrument, Catalog Number 07.00168.001, sold separately and as part of Zimmer Spine Trinica Anterior C
FDA device recall Z-1014-04 · posted 2005-02-24 · Terminated
Recall details
- Recalling firm
- Zimmer Spine, Inc.
- Reason for recall
- The recalled bone taps could break inside the vertebral body during the tapping process.
- Action taken
- Recall letters, dated May 25, 2004, request that the consignees locate and return the recalled devices.
- Root cause
- Other
- Status
- Terminated
- Product code
- HWX
- Quantity affected
- 55 units
- Distribution
- The product was shipped to Hawaii, New York, South Carolina, and South Dakota in the United States.
- Date initiated
- 2004-05-21
- Date posted
- 2005-02-24
- Date terminated
- 2005-11-03
- Location
- Minneapolis, MN
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| TRINICA SELECT ANTERIOR CERVICAL PLATE SYSTEM (K022344) | Centerpulse Spine-Tech, Inc. | 2002-09-24 |