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. 2,471 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,471 in last 12 months

Showing 3400134020 of 52,000 recalls

Medical DeviceAugust 3, 2016· LeMaitre Vascular, Inc.

Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome Recalled by LeMaitre Vascular, Inc. Due to...

The Issue: Wire which deploys the loop may be come detached at the handle causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· LeMaitre Vascular, Inc.

Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome without LeMills Recalled by LeMaitre...

The Issue: Wire which deploys the loop may be come detached at the handle causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· LeMaitre Vascular, Inc.

Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome Recalled by LeMaitre Vascular, Inc. Due to...

The Issue: Wire which deploys the loop may be come detached at the handle causing the...

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

Class II — Potential Health HazardOngoing
DrugAugust 2, 2016· Actavis Inc

Recalled Item: Acetasol HC (hydrocortisone and acetic acid otic solution USP) Recalled by...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugAugust 2, 2016· Actavis Inc

Recalled Item: Hydrocortisone and acetic acid otic solution Recalled by Actavis Inc Due to...

The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 2, 2016· Greatbatch Medical

Recalled Item: Greatbatch Recalled by Greatbatch Medical Due to On December 17, 2015,...

The Issue: On December 17, 2015, Greatbatch discovered that the Standard Offset Cup...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 2, 2016· Becton Dickinson & Company

Recalled Item: catalog # 405612 BD Spinal Anesthesia Tray 22G x 3.5 Recalled by Becton...

The Issue: A recall was initiated by Hospira, Inc. for several lots of 5% Lidocaine HCI...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Hologic, Inc

Recalled Item: SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI....

The Issue: Tip Breakage at the glue joint between the obturator body and tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Randox Laboratories Ltd.

Recalled Item: Randox Lipase (Colorimetric) Product Usage: A lipase test system is Recalled...

The Issue: According to the firm carry over was observed when the Lipase test is run...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.Plaza VB 10 A Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens is releasing a Customer Advisory Notice to explain meaning of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Alere San Diego, Inc.

Recalled Item: LDX Optical Check Cassettes (OCC) Model Number: 10-228 and 14-535 Recalled...

The Issue: Incorrect expiration date on the magnetic strip that does not match the...

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

Class III — Low RiskOngoing
Medical DeviceAugust 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo Plaza picture archiving and communication system (PAC) (PACS) intended...

The Issue: Siemens is releasing a Customer Advisory Notice to explain meaning of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Hologic, Inc

Recalled Item: SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI....

The Issue: Tip Breakage at the glue joint between the obturator body and tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2016· Bayer Healthcare

Recalled Item: Certegra Workstation used in conjunction with Medrad Stellant CT Injection...

The Issue: CertegraWorkstation when used in conjunction with the Medrad Stellant CT...

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

Class II — Potential Health HazardOngoing
DrugAugust 1, 2016· Spectrum Laboratory Products, Inc.

Recalled Item: Zinc Acetate Recalled by Spectrum Laboratory Products, Inc. Due to Does not...

The Issue: Does not meet monograph: product exhibits lead levels in excess of the USP...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 1, 2016· Isomeric Pharmacy Solution, LLC

Recalled Item: Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension...

The Issue: Lack of processing controls: Isomeric Pharmacy Solution, LLC is recalling...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Multix Fusion Stationary X-Ray System Product Usage: The Multix Fusion...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Multix Fusion VA10 Product Usage: The Multix Fusion VA10 system Recalled by...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: YSIO Max Product Usage: The Ysio Max is a radiographic Recalled by Siemens...

The Issue: Siemens became aware of a potential issue with the patient table for Ysio...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2016· Ethicon, Inc.

Recalled Item: ETHICON MERSILENE" Tape (also to as MERSILENETM Polyester Fiber Recalled by...

The Issue: ETHICON MERSILENE" Tape (also to as MERSILENETM Polyester Fiber Strip or...

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

Class II — Potential Health HazardOngoing