Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,740 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,740 in last 12 months

Showing 4728147300 of 52,000 recalls

Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System PS Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System CR Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: EZTest Steam Biological Indicator Recalled by Steritec Products Mfc. Co.,...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Radiometer America Inc

Recalled Item: pO2 D999 membrane units. Distributed by Radiometer America Recalled by...

The Issue: RADIOMETER became aware that the regarded lot pO2 units 942-042R0971 were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Getinge Assure Accufast BI Test Pack w/ 5 Controls Recalled by Steritec...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Cardinal Steam Biological Indicator Recalled by Steritec Products Mfc. Co.,...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Mesa Labs Smart-Read 10^5 EZ Test BI Test Pack Recalled by Steritec Products...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

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

Recalled Item: 00597603110 Articular Surface AC ART SURF 34/STRIPED YEL 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: 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· 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: 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· Baxter Healthcare Corp.

Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...

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· 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· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Sets The Paradigm infusion sets...

The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Medtronic is recalling...

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

Class I — Serious 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: 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· 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· Zimmer, Inc.

Recalled Item: 00595201201 Femur CR-FLEX POR 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: 00587806126 Patella MICRO POROUS PAT 26MM X 10MM 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