Zimmer Spine, Inc. ATO Drill Guide Kit (All Through One Drill Guides Set), model number 07.00860.001, product is packaged in trays. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ATO Drill Guide Kit (All Through One Drill Guides Set), model number 07.00860.001, product is packaged in trays.
Brand
Zimmer Spine, Inc.
Lot Codes / Batch Numbers
Serial Numbers: ATO-001 through ATO-0082
Products Sold
Serial Numbers: ATO-001 through ATO-0082
Zimmer Spine, Inc. is recalling ATO Drill Guide Kit (All Through One Drill Guides Set), model number 07.00860.001, product is packag due to To date, there has been one complaint reported. During a Trinica surgical case, the surgeon was provided a standard disposable, Trinica Drill Bit (pa. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
To date, there has been one complaint reported. During a Trinica surgical case, the surgeon was provided a standard disposable, Trinica Drill Bit (part number 07.00166.001) for use with the Trinica All Through One Drill Guide Instrumentation, instead of the ALL Through One Drill Bit. This enabled the physician to drill a few millimeters further than expected.
Recommended Action
Per FDA guidance
The product distributed to accounts will be returned to Zimmer Spine. Product will be quarantined pending investigation and determination of appropriate corrective action.
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