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 2076120780 of 52,000 recalls

DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by AuroMedics Pharma LLC...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Capsules 300 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: DG Health Acid Reducer Ranitidine Tablets 150 mg Recalled by AuroMedics...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Caspules 150 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Capsules 150 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Avanos Medical, Inc.

Recalled Item: Haylard Closed Suction System for Neonates/Pediatrics Recalled by Avanos...

The Issue: Avanos Medical has received reports stating that the central lumen of some 5...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Dako Denmark A/S

Recalled Item: Dako Autostainer instruments: Autostainer Link 48 Recalled by Dako Denmark...

The Issue: The Autostainer instrument may not have a syringe tray installed which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· King Systems Corp. dba Ambu, Inc.

Recalled Item: King Vision Video Adapter Size 1/2. Laryngoscope used to examine Recalled by...

The Issue: Exhibiting a reversed image. Although the image may appear normal, the users...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2019· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to...

The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Becton Dickinson & Company

Recalled Item: Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of...

The Issue: The indicator may show available charge when the battery is close to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Medacta Usa Inc

Recalled Item: Medacta Shoulder SYSTEM HUMERAL ANATOMICAL METAPHYSIS Recalled by Medacta...

The Issue: Certain lot numbers of the Medacta Humeral Anatomical Cementless Metaphysis...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo Recalled by Villa Sistemi Medicali S.P.A. Due to An amendment to the...

The Issue: An amendment to the IFU and Service Manual is being issued to prescribe the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Healix Knotless ADV BR 5.5 Suture Anchor Recalled by DePuy Mitek, Inc., a...

The Issue: Specific product codes and lots of the Mitek HEALIX ADVANCE" Knotless...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2019· Shimadzu Medical Systems

Recalled Item: Trinias DAP Meter Recalled by Shimadzu Medical Systems Due to The DAP meters...

The Issue: The DAP meters were found to be outside of tolerance.

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

Class II — Potential Health HazardOngoing