Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Nextgen Complete Knee Solution Femoral and Provisional Impactor/ Extractor Recalled by Zimmer Inc. Due to The design of the spring clip for the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zimmer Inc. directly.
Affected Products
Nextgen Complete Knee Solution Femoral and Provisional Impactor/ Extractor, REF 00-5901-026-00, Non-Sterile Zimmer, Warsaw Indiana The instrument is attached to the femoral implant or provisional to aid in positioning and inserting the components.
Quantity: 1662 units
Why Was This Recalled?
The design of the spring clip for the jaw assembly was updated in March 2011 due to fractures of the spring clip. Zimmer has received complaints for the spring clip fracturing on the updated design. The spring clip may fracture or fall off of the instrument during use, and a device fragment may be left in the surgical site. The risk of disassembly or fracture occurs when the instrument is typicall
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer Inc.
Zimmer Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report