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. 2,492 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,492 in last 12 months

Showing 2820128220 of 29,188 recalls

Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS Intact PINP Control Set Recalled by Immunodiagnostics Systems Ltd...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Recalled by...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS N-Mid¿ Osteocalcin Recalled by Immunodiagnostics Systems Ltd Due to...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Steris Corporation

Recalled Item: QKC1692E The QKC1692E Quick Connect device connects endoscopes to the...

The Issue: STERIS has been actively seeking devices for quick connect revalidation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS Urine BETA CrossLaps ELISA Recalled by Immunodiagnostics Systems Ltd Due...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS N-Mid¿ Osteocalcin Recalled by Immunodiagnostics Systems Ltd Due to...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Capsule Tech Inc.

Recalled Item: Capsule Neuron Docking Station Recalled by Capsule Tech Inc. Due to Capsule...

The Issue: Capsule Neuron Docking Station may experience a lost connection, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2012· Immunodiagnostics Systems Ltd

Recalled Item: IDS-iSYS Intact PINP Recalled by Immunodiagnostics Systems Ltd Due to It has...

The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Stryker Spine

Recalled Item: Stryker XIA 3 TORQUE WRENCH Manufactured by: Stryker Recalled by Stryker...

The Issue: Multiple complaints have reported the hex tip of the torque wrench...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Applied Medical Resources Corp

Recalled Item: Irrigation Catheters (Models IRR-XXX-XX): Model Numbers & Description:...

The Issue: Applied Medical is recalling specific lot numbers of its Vascular Catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· AGFA Corp.

Recalled Item: AGFA IMPAC CV DICOMStore with Media Purge Daemon (MPD) and Recalled by AGFA...

The Issue: Loss of patient data can occur under certain circumstances due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Applied Medical Resources Corp

Recalled Item: Embolectomy Catheters (Models A44XX Recalled by Applied Medical Resources...

The Issue: Applied Medical is recalling specific lot numbers of its Vascular Catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Integra LifeSciences Corporation

Recalled Item: Integra HRAIM Head Ring Assembly with Intubation Mounts The CRW Recalled by...

The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· AmeriWater Inc

Recalled Item: AmeriWater MRO Dialysis RO+ System Recalled by AmeriWater Inc Due to The...

The Issue: The firm was notified that a malfunction of the device was caused by an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Integra LifeSciences Corporation

Recalled Item: Integra CRW Precision Arc (CRWPRECISE) Recalled by Integra LifeSciences...

The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Stryker Spine

Recalled Item: SPECIALTY AUDIBLE TORQUE WRENCH Recalled by Stryker Spine Due to Multiple...

The Issue: Multiple complaints have reported the hex tip of the torque wrench...

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

Class II — Potential Health HazardOngoing