Reported Aug 8, 2012 · Terminated

Nextgen Complete Knee Solution Femoral and Provisional Impactor/ Extractor, REF 00-5901-026-00, Non-Sterile Zimmer,…

Zimmer Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Zimmer Inc. · 345 E Main St · Warsaw, IN · 46580-2746

Is this the product you have?

  • 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.
Lot codes and dates
    • Part 00-5901-026-00 Lot 11002148
    • 11002149
    • 11002791
    • 11002792
    • 11002831
    • 11003439
    • 11003449
    • 61800676
    • 61814993
    • 61909414
    • 61924920
    • 61980656
    • 61985378
    • 61988272
    • 61990656
    • 62003795
    • 62011220
    • 77000065
    • 77000573
    • 77000574
    • 77000575
    • 77000583
    • 77000654
    • 77000786
    • 77000787
    • 77000788
    • 77000789
    • 77000790
    • 77000795
    • 77000797
    • 77000798
    • 77000799
    • 77000804
    • 77000848
    • 77000849
    • 77000872
    • 77000873
    • 77001039
    • 77001048
    • 77001096
    • 77001097
    • 77001118
    • and 77001119
Amount recalled
1662 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was 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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 4, 2014 · Data as of Sep 19, 5:23 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.