Trinica Bone Tap Instrument, Catalog Number 07.00168.001, sold separately and as part of Zimmer Spine Trinica Anterior Cervical Plating Instrument sets (catalog numbers 07.00215.001 and 07.00546.001). Only the Trinica Bone Tap Instruments are being recalled from the sets.
This recall has been terminated (originally issued February 24, 2005).
- Company
- Zimmer Spine, Inc.
- Recall Initiated
- May 21, 2004
- Posted
- February 24, 2005
- Terminated
- November 3, 2005
- Recall Number
- Z-1014-04
- Quantity
- 55 units
- Firm Location
- Minneapolis, MN
- Official Source
- View on FDA website ↗
Reason for Recall
The recalled bone taps could break inside the vertebral body during the tapping process.
Distribution
The product was shipped to Hawaii, New York, South Carolina, and South Dakota in the United States.
Lot / Code Info
Lot P020077.
Root Cause
Other
Action Taken
Recall letters, dated May 25, 2004, request that the consignees locate and return the recalled devices.
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