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. 1,016 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,016 in last 12 months

Showing 27941–27960 of 52,000 recalls

DrugJanuary 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 40 mg Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System. 25 mcg/h Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System. 75 mcg/h Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 20 mg Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 10 mg Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack: 1) UDI-M535SAK3010 Recalled by NxStage Medical, Inc....

The Issue: May contain endotoxin levels which have been confirmed to exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Beckman Coulter Inc.

Recalled Item: AQUIOS CL Flow Cytometer System Recalled by Beckman Coulter Inc. Due to The...

The Issue: The device may process the same sample with two different sample IDs and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Philips Electronics North America Corporation

Recalled Item: Philips QCPR Meter - used with MRx Product Usage: The Recalled by Philips...

The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Philips Electronics North America Corporation

Recalled Item: Philips QCPR Meter - used with FR3 Product Usage: The Recalled by Philips...

The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Stryker Communications

Recalled Item: Berchtold Chromophare Ceiling Mounted Surgical Light System Recalled by...

The Issue: The device could have a missing spanner nut and snap ring which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound System Product Usage: The SC2000 ultrasound imaging...

The Issue: The application may underestimate the EROA (Effective Regurgitant Orifice...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: Biograph Horizon - PET/CT Recalled by Siemens Medical Solutions USA, Inc....

The Issue: Error introduced into PET images acquired and reconstructed with VJ20A...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2018· Stryker Communications

Recalled Item: Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel Recalled...

The Issue: The mounts on the monitor may have an insufficient (missing or incomplete) weld.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: Ray Station 4.9 Ray Station 5 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software issue with Center Beam in Field functionality. Issue can result in...

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

Class II — Potential Health HazardOngoing