Biomet U.K., Ltd.: 19 recalls on record

Recalls filed with 1 agency: FDA (19).

First recall on record: August 29, 2012. Most recent: October 3, 2018.

Risk classification: Class II: 19

Most recent recalls

DateAgencyProduct
October 3, 2018FDAHipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 3 Hole Plate …Z-3262-2018
March 1, 2017FDAOxford Partial Knee System Right Medial Tibial Trial Tray Size E Product Usage: Instrum…Z-1160-2017
March 1, 2017FDAOxford Partial Knee System Left Medial Tibial Trial Tray Size F Product Usage: Instrume…Z-1157-2017
March 1, 2017FDAOxford Partial Knee System Phase 3 Tibial Template Right Medial Size D Product Usage: …Z-1171-2017
March 1, 2017FDAOxford Partial Knee System Femoral Slap Hammer Product Usage: Instruments for use with …Z-1153-2017
March 1, 2017FDAOxford Partial Knee System Phase 3 Tibial Template Right Medial Size B Product Usage: I…Z-1175-2017
March 1, 2017FDAOxford Partial Knee System Left Medial Tibial Trial Tray Size B Product Usage: Instrume…Z-1167-2017
March 1, 2017FDAOxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage: Instruments for use…Z-1154-2017
March 1, 2017FDAOxford Partial Knee System Left Medial Tibial Trial Tray Size A Product Usage: Instru…Z-1159-2017
March 1, 2017FDAOxford Partial Knee System Right Medial Tibial Trial Tray Size F Product Usage: Instrum…Z-1156-2017
March 1, 2017FDAOxford Partial Knee System Right Medial Tibial Trial Tray Size C Product Usage: Instrum…Z-1164-2017
March 1, 2017FDAOxford Partial Knee System Phase 3 Tibial Template Right Medial Size C Product Usage: I…Z-1173-2017
March 1, 2017FDAOxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Instruments for use wit…Z-1170-2017
March 1, 2017FDAOxford Partial Knee System Right Medial Tibial Trial Tray Size C Oxford Partial Knee …Z-1165-2017
March 1, 2017FDAOxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage: Instrume…Z-1161-2017
March 1, 2017FDAOxford Partial Knee System Phase 3 Tibial Template Left Medial Size C Product Usage: In…Z-1172-2017
March 1, 2017FDAOxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Instruments for use wit…Z-1168-2017
April 24, 2013FDAREF 32-422760 Oxford Uni Knee System,Toffee Hammer, non-sterile, found in REF 32-422…Z-1124-2013
August 29, 2012FDAOxford Gap Gauge SML 3/4mm. The instrument is used for an intermediate check of the fl…Z-2224-2012

Questions about this company

How many recalls does Biomet U.K., Ltd. have?
Recalert has 19 U.S. recalls on record for Biomet U.K., Ltd., published between August 29, 2012 and October 3, 2018.
What was the most recent Biomet U.K., Ltd. recall?
FDA recall Z-3262-2018, published October 3, 2018: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 3 Hole Plate Item Number: 2110-135-003 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixat…
Which agencies have handled Biomet U.K., Ltd. recalls?
Biomet U.K., Ltd. appears as the recalling firm in recalls from: FDA (19).

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