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. 2,452 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,452 in last 12 months

Showing 3884138860 of 52,000 recalls

Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BEA Broth with Vancomycin container type: 13x100mm tube...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics VRE Broth Recalled by Hardy Diagnostics Due to Hardy...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
DrugJune 26, 2015· American Health Packaging

Recalled Item: Desmopressin Acetate Tablets Recalled by American Health Packaging Due to...

The Issue: Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted...

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2015· Ranbaxy Inc.

Recalled Item: Absorica (isotretinoin) Capsules Recalled by Ranbaxy Inc. Due to Undeclared...

The Issue: Incorrect/Undeclared Excipients: Product contains undeclared FD&C Yellow No....

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 26, 2015· Vitamin Cottage Natural Food Markets, Inc.

Recalled Item: Natural Grocers Caribbean Fruit & Nut Mix Recalled by Vitamin Cottage...

The Issue: Vitamin Cottage Natural Food Markets, Inc is recalling one lot of Natural...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 25, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON S 1000 Recalled by Siemens Medical Solutions USA, Inc. Due to...

The Issue: Potential measurement error on ACUSON S Family ultrasound system when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON S2000 and ACUSON S3000 ultrasound systems with the Virtual Recalled...

The Issue: Potential measurement error on ACUSON S Family ultrasound system. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· Zimmer Surgical Inc

Recalled Item: 30inch Dual Port/Single Bladder Disposable Tourniquet Cuff with PLC Recalled...

The Issue: The inside of the folded Instructions For Use (IFU) pamphlet was missing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Prism Medical P-600 Portable Ceiling Lift Recalled by ErgoSafe Products, LLC...

The Issue: There is a potential the sling loops may not stay attached to the carry bar...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes TI Matrix Pre-Bent Maxillary Plate / 2mm ADVMNT/0.8mm THK/L Recalled...

The Issue: The affected part and lot numbers of the TI Matrix Pre-Bent Maxillary Plates...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Prism Medical P-440 Portable Ceiling Lift Recalled by ErgoSafe Products, LLC...

The Issue: There is a potential the sling loops may not stay attached to the carry bar...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· Synthes (USA) Products LLC

Recalled Item: 16mm Chisel Blade Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was discovered that a 10mm Chisel Blade was etched as a 16mm Chisel Blade.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· EKOS Corporation

Recalled Item: The EKOS EkoSonic Control Unit is intended exclusively for use Recalled by...

The Issue: The Connector Interface Cable (CIC) was not recognized by the EkoSonic PT-3B...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· Zimmer Surgical Inc

Recalled Item: 18inch Dual Port/Single Bladder Disposable Tourniquet Cuff Recalled by...

The Issue: The inside of the folded Instructions For Use (IFU) pamphlet was missing the...

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

Class II — Potential Health HazardOngoing
DrugJune 24, 2015· Teva Pharmaceuticals USA

Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications: out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2015· Actavis Laboratories, FL, Inc.

Recalled Item: Desmopressin Acetate Tablets Recalled by Actavis Laboratories, FL, Inc. Due...

The Issue: Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 23, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer SST Plus Blood Collection Tubes Recalled by Becton Dickinson &...

The Issue: Some of the tubes were manufactured with stoppers that did not meet current...

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

Class III — Low RiskOngoing
Medical DeviceJune 23, 2015· O-Two Medical Technologies, Inc.

Recalled Item: O-Two Adult Ventilation Timer Recalled by O-Two Medical Technologies, Inc....

The Issue: Malfunction of an O-Two Adult Ventilation Timer, where the flash rate of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Draeger Medical, Inc.

Recalled Item: Fabius MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due to the...

The Issue: the Fabius MRI or parts of the system were attracted by the magnetic field...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems with software versions...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

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

Class II — Potential Health HazardOngoing