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. 2,848 recalls have been distributed to Virginia in the last 12 months.
Showing 1621–1640 of 29,425 recalls
Recalled Item: Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial...
The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allon 2001. Part Number: 200-00263 Recalled by Belmont Instrument LLC Due to...
The Issue: An investigation into a report of the patient wrap (ThermoWrap), used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Evolution Upgrade 3.0T Recalled by Philips North America Llc...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 3.0T CX Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 1.5T CX Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: MR 7700 Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia Elition X Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 3.0T Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia 1.5T S Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: SmartPath to dStream for 3.0T Recalled by Philips North...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia Ambition X Recalled by Philips North America Llc Due...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia Elition S Recalled by Philips North America Llc Due to...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: SmartPath to Ingenia Elition X Recalled by Philips North...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Ingenia Ambition S Recalled by Philips North America Llc Due...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Evolution Upgrade 1.5T Recalled by Philips North America Llc...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: SmartPath to dStream for XR and 3.0T Recalled by Philips North...
The Issue: Potential for alignment errors in the cross line functionality when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.