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. 1,916 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,916 in last 12 months

Showing 2676126780 of 29,228 recalls

Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597201101 Femur CR POROUS FEM COMP SIZE 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: 00597003109 Articular Surface CR ART SURF 34/STRIPE YEL 9 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: 00595202010 Articular Surface XLPE CR ART SURF 1 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: 00595204110 Articular Surface XLPE CR ART SURF 5-6/STRGRN 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: 00597103110 Provisional CR ART SURF PROV 34/STR YEL 10 Recalled by Zimmer,...

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: 00597206126 Patella ALL POLY PAT COMP MICRO 26DIA 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: 00597001303 Femur CR PRC FEM COMP SIZE CML Rx Recalled by Zimmer, Inc. Due...

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: 90597002009 Articular Surface CR ART SURF 12/PURPLE 09MM Recalled by Zimmer,...

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: 90597004109 Articular Surface CR ART SURF AE56/STR GRN 09MM 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: 00595601201 Femur CR-FLEX OPT FEM B-L Rx Sterile 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: 00597002009 Articular Surface CR ART SURF 12/PURPLE 9 Recalled by Zimmer,...

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: 65595201201 Femur CR-FLEX POR HATCP FEM B-L Rx Recalled by Zimmer, Inc. Due...

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: 90597003109 Articular Surface CR ART SURF 34/STR YEL 09MM 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· Baxter Healthcare Corp.

Recalled Item: Brand Name: Regional Analgesia Infusor System with Patient Control....

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Infusor SV and LV Elastomeric Infusion Devices. Indicated...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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