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. 2,535 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,535 in last 12 months

Showing 2258122600 of 29,188 recalls

Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to Error in...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to Error in...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to Error in...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Elite Biomedical Solutions LLC

Recalled Item: Alaris Medley LVP Bezel Assembly. Intended use to hold platen Recalled by...

The Issue: Administration of inappropriate quantities of fluid can result, with the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD Recalled by...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker SelectCore Variable Throw Biopsy Device Recalled by Stryker...

The Issue: Stryker Instruments is recalling the Stryker SelectCore Variable Throw...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2015· Alcon Research, Ltd.

Recalled Item: Accurus 2500 Standalone Vitreous Probe Recalled by Alcon Research, Ltd. Due...

The Issue: Insufficient seal on the outside packaging, potentially affecting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2015· ArthroCare Corporation

Recalled Item: EVac 70 XTRA with Integrated Cable and PROcise EZ View Recalled by...

The Issue: Wands inspected with the adaptor fixture were released to the field not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Stryker Sustainability Solutions

Recalled Item: Fios First Entry Recalled by Stryker Sustainability Solutions Due to Stryker...

The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Elekta, Inc.

Recalled Item: Laksell GammaPlan Recalled by Elekta, Inc. Due to Memory can become...

The Issue: Memory can become corrupted when creating a fused study via drag and drop in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Stryker Sustainability Solutions

Recalled Item: Optical Access System Recalled by Stryker Sustainability Solutions Due to...

The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Stryker Sustainability Solutions

Recalled Item: Cannula and Seal Recalled by Stryker Sustainability Solutions Due to Stryker...

The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing