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 2086120880 of 29,425 recalls

Medical DeviceMay 11, 2016· Synthes (USA) Products LLC

Recalled Item: Norian Drillable Inject 10 CC-Sterile Recalled by Synthes (USA) Products LLC...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2016· Medical Vision Ab

Recalled Item: Double Pump RF Patient Cassette Recalled by Medical Vision Ab Due to...

The Issue: Sterility of device may be compromised due to sterile package breakage.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2016· Integra LifeSciences Corp.

Recalled Item: TS Series Depth Gauge for Integra Ti6 Internal Fixation System Recalled by...

The Issue: As a result of an internal investigation of a non-conformance it has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· Immuno-Mycologics, Inc

Recalled Item: Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal...

The Issue: The device was found to have bacterial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· GE Healthcare, LLC

Recalled Item: Optima 1.5T MR430s MR Scanner Recalled by GE Healthcare, LLC Due to The gas...

The Issue: The gas venting may not occur properly. A site reported a magnet quenching...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products AFP Reagent Pack Recalled by ORTHO-CLINICAL...

The Issue: Ortho Clinical Diagnostics (OCD) confirmed that specific lots of VITROS...

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

Class III — Low RiskOngoing
Medical DeviceMay 9, 2016· GE Healthcare, LLC

Recalled Item: MSK 1.5T Extreme MR Scanner Recalled by GE Healthcare, LLC Due to The gas...

The Issue: The gas venting may not occur properly. A site reported a magnet quenching...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· GE Healthcare, LLC

Recalled Item: GE Revolution CT The system is intended for head Recalled by GE Healthcare,...

The Issue: GEHC has become aware of a potential safety issue in the Revolution CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2016· Medtronic Navigation, Inc.

Recalled Item: Visualase Cooled Laser Applicator System (VCLAS). The VCLAS system consists...

The Issue: Potential for the Visualase Cooled Laser Applicator System (VCLAS) catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2016· Custom Ultrasonics, Inc.

Recalled Item: The System 83 Plus Recalled by Custom Ultrasonics, Inc. Due to To warn...

The Issue: To warn customers that Custom Ultrasonics, Inc. System 83 Plus AERs should...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2016· BEST THERATRONICS LTD.

Recalled Item: Best Theratronics cabinet x-ray systems intended for use in the Recalled by...

The Issue: It was discovered that both the new device and the predicate device failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2016· Leica Biosystems Richmond Inc.

Recalled Item: Ariol is an automated scanning microscope and image analysis system....

The Issue: An issue during the manufacturing process caused systems to have an...

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

Class III — Low RiskOngoing
Medical DeviceMay 5, 2016· Ellipse A/S

Recalled Item: Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser...

The Issue: Failure to provide the required instructions specifying a procedure and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker PowerPRO (XT Recalled by Stryker Medical Division of Stryker...

The Issue: Complaints of smoke coming from the foot end of the cot. This reportedly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2016· Ellipse A/S

Recalled Item: Ellipse ND: YAG Laser applicator for Ellipse Nordlys system Medical Recalled...

The Issue: Failure to provide the required instructions specifying a procedure and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Cordis Corporation

Recalled Item: Cordis PRECISE (R) RX Nitinol Stent System (Biliary) Recalled by Cordis...

The Issue: Inability to deploy the stent or partial stent deployment.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Zimmer Plates and Screws (ZPS) 3.5 mm Cortical Screw SelfTapping Recalled by...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: ITST intertrochanteric/subtrochanteric fixation 4.5 mm diameter cortical...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Herbert Cannulated Bone Screw System Recalled by Zimmer Manufacturing B.V....

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2016· Zimmer Manufacturing B.V.

Recalled Item: Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone...

The Issue: A small hole may be present in the inner tray of specific lots of sterile...

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

Class II — Potential Health HazardOngoing