Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,455 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,455 in last 12 months

Showing 4882148840 of 53,528 recalls

Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00595001201 Femur CR-FLEX PCT FEM B-L Rx Recalled by Zimmer, Inc. Due to...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597604110 Articular Surface AC ART SURF 56/STRIPED GRN 10 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 90595204117 Articular Surface XLPE CR ART SURF AE56/STGRN 17 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 65597201131 Femur CR POR FEM SURF HDN HATCP AML Rx Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597001131 Femur CR PRC SURF HDN FEM CO-NID AML Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 90595203117 Articular Surface XLPE CR ART SURF AE34/STYEL 17 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Programmable Infusion Pump- Implantable for the intrathecal...

The Issue: Miscalibrated Fill Level Sensor may affect dosing level

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc....

The Issue: Miscalibrated Fill Level Sensor may affect dosing level

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Fixed Bearing Partial Knee Cemented Lateral Tibia Size Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Fixed Bearing Partial Knee Cemented Lateral Tibia Size Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Biomet, Inc.

Recalled Item: Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Recalled by Biomet,...

The Issue: Biomet investigation found the design of the tibial bearing creates the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing