Product Recalls in Virginia

Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,997 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,997 in last 12 months

Showing 1476114780 of 29,425 recalls

Medical DeviceFebruary 25, 2019· Nidek, Inc.

Recalled Item: NIDEK Specular Microscope Recalled by Nidek, Inc. Due to The electromagnetic...

The Issue: The electromagnetic noise exceeded the upper limit of the Electromagnetic...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 25, 2019· Cook Medical Incorporated

Recalled Item: Cook Celect Platinum Vena Cava Filter Set for Femoral and Jugular Vein...

The Issue: Updates to the Instructions for Use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 25, 2019· Cook Medical Incorporated

Recalled Item: Cook Celect Platinum Vena Cava Filter Set for Jugular Vein Approach Recalled...

The Issue: Updates to the Instructions for Use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 25, 2019· Cook Medical Incorporated

Recalled Item: Gunther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach...

The Issue: Updates to the Instructions for Use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 25, 2019· Cook Medical Incorporated

Recalled Item: Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach Recalled by...

The Issue: Updates to the Instructions for Use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 25, 2019· Cook Medical Incorporated

Recalled Item: Cook Celect Platinum Vena Cava Filter Set for Femoral Vein Approach Recalled...

The Issue: Updates to the Instructions for Use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 25, 2019· Cook Medical Incorporated

Recalled Item: Gunther Tulip Vena Cava Filter Set for Jugular Vein Approach Recalled by...

The Issue: Updates to the Instructions for Use.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 22, 2019· Luminex Molecular Diagnostics

Recalled Item: xTAG Gastrointestinal Pathogen Panel intended for the simultaneous...

The Issue: Reports have been received of lower MS2 MFI values when using the panel.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2019· Keystone Dental Inc

Recalled Item: Paltop Fully Guided Surgical Kit- containing the 1.25mm Hex Driver Recalled...

The Issue: Paltop Surgical Kits contain 1.25mm Hex Driver(s) which may have a slightly...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2019· Keystone Dental Inc

Recalled Item: Paltop Premium Surgical Kit-containing the 1.25mm Hex Driver For surgical...

The Issue: Paltop Surgical Kits contain 1.25mm Hex Driver(s) which may have a slightly...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2019· GE Healthcare, LLC

Recalled Item: Integrated ECG cable with 3-lead leadwires labeled as the following:...

The Issue: The Integrated ECG cable with 3-lead leadwires can short circuit during...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 22, 2019· Keystone Dental Inc

Recalled Item: Paltop 1.25 Hex Drivers Recalled by Keystone Dental Inc Due to Paltop...

The Issue: Paltop Surgical Kits contain 1.25mm Hex Driver(s) which may have a slightly...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2019· Keystone Dental Inc

Recalled Item: Paltop 1.25 Hex Drivers Recalled by Keystone Dental Inc Due to Paltop...

The Issue: Paltop Surgical Kits contain 1.25mm Hex Driver(s) which may have a slightly...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2019· ArthroCare Corporation

Recalled Item: Smith&Nephew SmartStitch PerfectPasser Connector Recalled by ArthroCare...

The Issue: The voluntary recall is being initiated due to a manufacturing error...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: icumedical ChemoLock Closed Vial Spike w/Skirt Recalled by ICU Medical, Inc....

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: SetSource ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: icumedical ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: icumedical ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: icumedical Oncology Kit w/12" (30cm) Ext Set w/Spiros w/Red Cap Recalled by...

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2019· ICU Medical, Inc.

Recalled Item: icumedical ChemoLock Recalled by ICU Medical, Inc. Due to There is a...

The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...

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

Class I — Serious Health HazardOngoing