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. 2,509 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,509 in last 12 months

Showing 2292122940 of 52,000 recalls

Medical DeviceMay 21, 2019· DRG Instruments GmbH

Recalled Item: DRG Salivary Testosterone ELISA- IVD for the detection of Testerone Recalled...

The Issue: Salivary assay may observe a higher percentage of samples with 0 pg/ml...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· Medtronic Inc

Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling

The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· Medtronic Inc

Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling

The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· GE Healthcare, LLC

Recalled Item: LVivo EF app on Vscan Extend. Sold under the following Recalled by GE...

The Issue: Overestimation bias in automatically calculated ejection fraction (EF)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· Medtronic Inc

Recalled Item: Mosaic 310 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling

The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2019· Medtronic Inc

Recalled Item: Hancock II T510 Bioprosthesis Recalled by Medtronic Inc Due to Mislabeling

The Issue: Fifteen affected devices were distributed worldwide, which were mislabeled...

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

Class II — Potential Health HazardOngoing
DrugMay 21, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: PROCHLORPERAZINE EDISYLATE INJECTION Recalled by Heritage Pharmaceuticals,...

The Issue: Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 21, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: AMIKACIN SULFATE INJECTION Recalled by Heritage Pharmaceuticals, Inc. Due to...

The Issue: Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 21, 2019· Dutch Ophthalmic USA, Inc.

Recalled Item: The device is a 25-gauge infusion line that is part Recalled by Dutch...

The Issue: Labeled 25-gauge surgical pack, TDC Vitrectomy Pack VGPC 25g, containing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2019· Opternative Inc

Recalled Item: The Visibly Online Vision Test which is part of Recalled by Opternative Inc...

The Issue: Lack of 510K clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2019· Medtronic Inc.

Recalled Item: Guardian Connect App CSS7200 iOS and Guardian Connect Transmitter GST4C...

The Issue: Customers using the firm's continuous glucose monitoring system application...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86682003 Product...

The Issue: Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product...

The Issue: Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series...

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

Class II — Potential Health HazardOngoing
FoodMay 20, 2019· Reily Foods Co., Inc

Recalled Item: Blue Plate Light Mayonnaise 30oz Recalled by Reily Foods Co., Inc Due to...

The Issue: Yeast presence that resulted in gas formation causing bottles to bloat and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMay 20, 2019· Reily Foods Co., Inc

Recalled Item: Blue Plate Light Olive Oil Mayonnaise 30oz / 18oz Recalled by Reily Foods...

The Issue: Yeast presence that resulted in gas formation causing bottles to bloat and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
DrugMay 20, 2019· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA45 CT AR MD THK REL Recalled by Covidien LLC Due to The device may be...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 45 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 CURVED TIP ART MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing