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. 1,943 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,943 in last 12 months

Showing 1758117600 of 29,425 recalls

Medical DeviceSeptember 25, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Nonvented...

The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier IV in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Guangzhou Improve Medical Instruments Co., Ltd.

Recalled Item: Prevent G Safety Winged Blood Collection Set Glide - Rx Recalled by...

The Issue: Complain due to the hub needle came out when the nurse draw the blood and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Circulatory Technology Inc

Recalled Item: Better-Bladder cardiopulmonary bypass blood reservoir Recalled by...

The Issue: The device is used as part of extracorporeal membrane oxygenation (ECMO)...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier I in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier V in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Circulatory Technology Inc

Recalled Item: **Recall Expanded to add these models: Bigger Better-Bladder cardiopulmonary...

The Issue: The device is used as part of extracorporeal membrane oxygenation (ECMO)...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier III in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier II in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2017· Medtronic Neuromodulation

Recalled Item: Medtronic Ascenda(R) Intrathecal Catheter Recalled by Medtronic...

The Issue: There is a possibility that specific lots of catheters that have recently...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 21, 2017· Covidien LLC

Recalled Item: GastriSail" Gastric Positioning Device Product Usage: The GastriSail gastric...

The Issue: Reports of gastric or esophageal perforation occurring in procedures where...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Intuitive Surgical, Inc.

Recalled Item: daVinci X EndoWrist(R) Stapler 45 Recalled by Intuitive Surgical, Inc. Due...

The Issue: Specific da Vinci Xi EndoWrist Stapler 45 instruments are potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing