Zimmer Inc. Zimmer TM-400 Broach Handle; Part No. 96-210-10001. The product is a surgical instrument for use in conjunction with Zimmer TM-400 Trabecular Metal implants during spinal surgery. The Broach Handle threads onto various broaches and trial implants. The handle with these broaches or trials attached is used to prepare and measure a vertebral space to accept a TM-400 Trabecular Metal implant. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Zimmer TM-400 Broach Handle; Part No. 96-210-10001. The product is a surgical instrument for use in conjunction with Zimmer TM-400 Trabecular Metal implants during spinal surgery. The Broach Handle threads onto various broaches and trial implants. The handle with these broaches or trials attached is used to prepare and measure a vertebral space to accept a TM-400 Trabecular Metal implant.
Brand
Zimmer Inc.
Lot Codes / Batch Numbers
All lots.
Products Sold
All lots.
Zimmer Inc. is recalling Zimmer TM-400 Broach Handle; Part No. 96-210-10001. The product is a surgical instrument for use in due to The broach handle may fracture at the threaded tip during use, which would result in surgical intervention to retrieve the broach or the trial as the . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The broach handle may fracture at the threaded tip during use, which would result in surgical intervention to retrieve the broach or the trial as the threaded tip fragment prevents attachment of another handle to retrieve the device.
Recommended Action
Per FDA guidance
Distributors and user accounts were notified by "Urgent: Medical Device Recall" letter dated April 29, 2009. The letter described the affected product, reason for recall, health risks, and action for consignees. Distributors were instructed to retrieve the devices and to return them to Zimmer no later than May 13, 2009. This instrument recall will result in an inability to implant the associated devices until a new instrument becomes available. For questions or assistance about the recall please contact Zimmer Spine by calling 800-777-7505.
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