Reported Nov 7, 2012 · Terminated

Knee Components

Wright Medical Technology 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: Wright Medical Technology Inc · 5677 Airline Rd · Arlington, TN · 38002-9501

Is this the product you have?

72 of 72 products

Products covered by this recall
#Product as published
1Lot Number X02383380 INSERT TIBIAL "913 PCR" T.1 - EP.10-, PGA00050
2Lot Numbers: V11272719, W02300988, W09372781, W09372781, and W10372876 INSERT TIBIAL "913 PCR" T.1 - EP.14-, PGA00054
3Lot Number: V0266952 INSERT TIBIAL "913 PCR" T.2 - EP.10-, PGA00080
4Lot Numbers: X02396582, X05401377, and W01287345 INSERT TIBIAL "913 PCR" T.3 - EP.10-, PGA00110
5Lot Numbers: W09359102, X03396584, and W1166335 INSERT TIBIAL "913 PCR" T.5 - EP.14-, PGA00174
6Lot Number: W0675535 PLATEAU TIBIAL "913" T.4 MOINS , PGA00216
7Lot Number: X10391238 PLATEAU TIBIAL "913" T.5 MOINS , PGA00218
8Lot Numbers: V0379902 and V0381596 PLATEAU TIBIAL "913" T.1 , PGA00230
9Lot Numbers: W05327837 and W0779903 PLATEAU TIBIAL "913" T.2 PLUS , PGA00252
10Lot Number: X06391241 TIGE INTRAMEDULLAIRE "913" D=16 L=75, PGA00716
11Lot Number: X02382967 TIGE INTRAMEDULLAIRE "913" D=12 L=125, PGA00752
12Lot Number: W06322599 TIGE INTRAMEDULLAIRE "913" D=14 L=125, PGA00754
13Lot Number: V12272733 TIGE INTRAMEDULLAIRE "913" D=16 L=125, PGA00756
14Lot Number: V12272734 TIGE INTRAMEDULLAIRE "913" D=18 L=125, PGA00758
15Lot Number: W04336344 TIGE DE REPRISE FEMO/TIB. "913" D=14 L=75, PGA00814
16Lot Number: V0767876 TIGE DE REPRISE FEMO/TIB. "913" D=16 L=75, PGA00816
17Lot Number: V0767877 CALE TIBIALE "913" T.1 -EP.8- , PGA00950
18Lot Number: W0380839 CALE TIBIALE "913" T.2 -EP.8- , PGA00952
19Lot Number: V0773498 and V0973301 INSERT TIBIAL "913 RS" T.1 - EP.10-, PGA14010
20Lot Number: V0782533 INSERT TIBIAL "913 RS" T.1 - EP.12-, PGA14012
Amount recalled
729 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

There may be inaccuracies on the labeled shelf life on all products packaged at the Toulon, France facility.

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 Jan 7, 2014 · Data as of Sep 19, 5:28 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.