Recall archive
3 recalls · page 1 of 1
Reported Mar 1, 2017
Oxford Knee System Tibial Resector Body Tube & Guides Product Usage: Instruments for use with the Oxford Uni Partial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet U.K., Ltd.
Matched: Brand · Reason for recall — Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the…
23 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2013
REF 32-422760 Oxford Uni Knee System,Toffee Hammer, non-sterile, found in REF 32-422763 Oxford Mlcroplasty Knee System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet U.K., Ltd.
Matched: Brand — Investigation of complaints found excessive use of the instrument could result in cracking on the weld between the head and the handle, which could…
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Oxford Gap Gauge SML 3/4mm. The instrument is used for an intermediate check of the flexion and extension gaps when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet U.K., Ltd.
Matched: Brand — A drafting error during an unrelated design change has led to 4 misleading dimensions on the drawing. The CAD model remained the same thickness but…
FDA (openFDA device enforcement)
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