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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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00-5952-31-12, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Retai...
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2
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05/14/2012
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Zimmer Inc.
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00-5970-031-23, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta...
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2
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05/14/2012
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Zimmer Inc.
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00-5972-031-23, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta...
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2
|
05/14/2012
|
Zimmer Inc.
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00-5976-031-10, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta...
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2
|
05/14/2012
|
Zimmer Inc.
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00-5976-031-12, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta...
|
2
|
05/14/2012
|
Zimmer Inc.
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00-5976-031-14, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta...
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2
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05/14/2012
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Zimmer Inc.
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00-5976-031-17, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta...
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2
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05/14/2012
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Zimmer Inc.
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00-5976-031-20, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta...
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2
|
05/14/2012
|
Zimmer Inc.
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00-5976-031-23, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta...
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2
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05/14/2012
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Zimmer Inc.
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Knee Arthro Pack and Knee Arthro Pack II - contains Devon Light Glove
Used during surgery
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2
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07/07/2015
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Stradis Healthcare, LLC.
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