Biomet U.K recalls

Biomet U.K has 26 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 1 Mar 2017. The most frequent reason is lead & heavy metals.

Total recalls26since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 1 Mar 2017

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 26 100%Class III 0 0%

Why biomet u.k is recalled

Product types

By year

All biomet u.k recalls, newest first

26 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIOxford Unicompartmental Knee Phase 3 Shim Size recalled by Biomet U.KBiomet U.KLead & Heavy Metals14 states
DeviceCLASS IIOxford Knee System Tibial Resector Body Tube & Guides recalledBiomet U.KLead & Heavy Metals14 states
DeviceCLASS IIOxford Partial Knee System Right Medial Tibial Trial Tray Size D recalledBiomet U.KLead & Heavy Metals14 states
DeviceCLASS IIOxford Partial Knee System Phase 3 Tibial Template Right recalledBiomet U.KLead & Heavy Metals14 states
DeviceCLASS IIOxford Partial Knee System Right Medial Tibial Trial Tray Size B recalledBiomet U.KLead & Heavy Metals14 states
DeviceCLASS IIOxford Partial Knee System Right Medial Tibial Trial Tray Size recalledBiomet U.KLead & Heavy Metals14 states
DeviceCLASS IIOxford Partial Knee System Left Medial Tibial Trial Tray Size D recalledBiomet U.KLead & Heavy Metals14 states
DeviceCLASS IIOxford Partial Knee System Phase 3 Tibial Template Left recalledBiomet U.KLead & Heavy Metals14 states
DeviceCLASS IIOxford Partial Knee System Phase 3 Tibial Template Right recalledBiomet U.KLead & Heavy Metals14 states
DeviceCLASS IIOxford Unicompartmental Knee Phase 3 Tibial Impactor recalledBiomet U.KLead & Heavy Metals14 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.