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. 1,820 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,820 in last 12 months

Showing 3216132180 of 52,000 recalls

Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core128 X-Ray Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity CT X-Ray Recalled by Philips Electronics North...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance iCT X-Ray Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Potassium Chloride Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: Defective Container: Leakage of unit dose cups that may occur at the seal.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution Recalled by...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Metoclopramide Oral Solution Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Phenytoin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 17, 2017· Medtronic Neurosurgery

Recalled Item: Medtronic Strata II / Strata NSC Valves (includes Burr Hole Recalled by...

The Issue: Medtronic Neurosurgery initiated a recall after receiving five (5) Product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2017· OriGen Biomedical, Inc.

Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...

The Issue: Clamping the clear tube very close to the blue hub may cause a localized...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 17, 2017· OriGen Biomedical, Inc.

Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...

The Issue: Clamping the clear tube very close to the blue hub may cause a localized...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 17, 2017· Pentax of America Inc

Recalled Item: Video Duodenoscope These instruments are intended to provide optical...

The Issue: Pentax initiated a field correction/safety alert for two (2) models of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2017· OriGen Biomedical, Inc.

Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...

The Issue: Clamping the clear tube very close to the blue hub may cause a localized...

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

Class I — Serious Health HazardOngoing