Zimmer Spine, Inc. 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Zimmer Spine, Inc.
Lot Codes / Batch Numbers
Lot P020077.
Products Sold
Lot P020077.
Zimmer Spine, Inc. is recalling Trinica Bone Tap Instrument, Catalog Number 07.00168.001, sold separately and as part of Zimmer Spin due to The recalled bone taps could break inside the vertebral body during the tapping process.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The recalled bone taps could break inside the vertebral body during the tapping process.
Recommended Action
Per FDA guidance
Recall letters, dated May 25, 2004, request that the consignees locate and return the recalled devices.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026