Depuy Orthopaedics Inc. Recalls — U.S. Recall Records

Recall history in this database

Classification mix: Class II: 85.

Medical DeviceJul 30, 2014

DePuy Orthopaedics RECLAIM Taper Protector Sleeve recall — FDA Z-2082-2014

The product can be difficult to remove from the Distal Stem both out of the package and after proximal reaming.

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Medical DeviceJul 30, 2014

DePuy Orthopaedics RECLAIM DISTAL TAPERED Distal Stem, various sizes recall — FDA Z-2084-2014

The product can be difficult to remove from the Distal Stem both out of the package and after proximal reaming.

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Medical DeviceApr 16, 2014

DePuy Orthopaedics GLOBAL Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Part # recall — FDA Z-1437-2014

Urgent Device Correction notifications are being sent to USA distributors with follow-up to surgeons concerning updated surgical techniques stressing the possibility of the shoulder pin…

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Medical DeviceMar 19, 2014

DePuy Orthopaedics REF 623411 R S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented recall — FDA Z-1206-2014

DePuy Orthopaedics has identified the potential for holes to develop in the inner and outer flexible pouches that form the sterile barrier for S-ROM Noiles Rotating Hinge Femur with Pin…

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Medical DeviceMar 19, 2014

DePuy Orthopaedics REF 623401 R, S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge recall — FDA Z-1204-2014

DePuy Orthopaedics has identified the potential for holes to develop in the inner and outer flexible pouches that form the sterile barrier for S-ROM Noiles Rotating Hinge Femur with Pin…

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Medical DeviceMar 19, 2014

DePuy Orthopaedics REF 623411 L, S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge recall — FDA Z-1205-2014

DePuy Orthopaedics has identified the potential for holes to develop in the inner and outer flexible pouches that form the sterile barrier for S-ROM Noiles Rotating Hinge Femur with Pin…

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Medical DeviceMar 19, 2014

DePuy Orthopaedics REF 623401 L S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented recall — FDA Z-1203-2014

DePuy Orthopaedics has identified the potential for holes to develop in the inner and outer flexible pouches that form the sterile barrier for S-ROM Noiles Rotating Hinge Femur with Pin…

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Medical DeviceMar 19, 2014

DePuy Orthopaedics REF 623421 L S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented recall — FDA Z-1207-2014

DePuy Orthopaedics has identified the potential for holes to develop in the inner and outer flexible pouches that form the sterile barrier for S-ROM Noiles Rotating Hinge Femur with Pin…

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Medical DeviceMar 19, 2014

DePuy Orthopaedics REF 623421 RS-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented recall — FDA Z-1208-2014

DePuy Orthopaedics has identified the potential for holes to develop in the inner and outer flexible pouches that form the sterile barrier for S-ROM Noiles Rotating Hinge Femur with Pin…

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Medical DeviceMar 5, 2014

DePuy Orthopaedics PFC SIGMA Cruciate Retaining (CR) recall — FDA Z-1077-2014

Knee implant femoral devices were found to have anomalous microstructure. Porosity and the presence of blocky carbides, within the cobalt chrome part, can decrease the overall fatigue…

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Medical DeviceDec 4, 2013

DePuy Orthopaedics SIGMA LCS HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 4-7 HP M.B.T recall — FDA Z-0423-2014

DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP M.B.T. Keel Punch Knee Instrument because of the potential for tabs on the connection end to fracture and be left…

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Medical DeviceDec 4, 2013

DePuy Orthopaedics SIGMA LCS HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 2-3 HP M.B.T recall — FDA Z-0422-2014

DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP M.B.T. Keel Punch Knee Instrument because of the potential for tabs on the connection end to fracture and be left…

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Medical DeviceDec 4, 2013

DePuy Orthopaedics SIGMA LCS HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 2-3 HP M.B.T recall — FDA Z-0419-2014

DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP M.B.T. Keel Punch Knee Instrument because of the potential for tabs on the connection end to fracture and be left…

Class IIFDA: TerminatedDePuy Orthopaedics, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Depuy Orthopaedics Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.