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. 1,161 recalls have been distributed to Virginia in the last 12 months.
Showing 1561–1580 of 29,425 recalls
Recalled Item: Philips VL13-5 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...
The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips S7-3t Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...
The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...
The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips eL18-4 EMT Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips XL14-3 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips C5-1 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL...
The Issue: Package labeling for Altivate Reverse Torx Peripheral screw contains a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Long Nail Recalled by Stryker GmbH Due to Investigation confirmed that the...
The Issue: Investigation confirmed that the GAMMA4 Right Long Nail was manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe...
The Issue: Due to an error in assembly of the thermistor within some units, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips L9-3 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips L12-4 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips L8-4 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STICK Recalled by Microbiologics Inc Due to Affected products were...
The Issue: Affected products were packaged with the incorrect KWIK STIK assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm O2 Imaging System. Mobile X-Ray System. Recalled by Medtronic...
The Issue: A mechanical component that supports the O2 gantry to the support structure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing BD Insyte Autoguard Shielded IV...
The Issue: Medline Industries, LP. is issuing a recall for specific Medline kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing BD Insyte Autoguard Shielded IV...
The Issue: Medline Industries, LP. is issuing a recall for specific Medline kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE¿ device is...
The Issue: Due to a software bug the robotic arm may incorrectly guide the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroMyst Applicator Recalled by Integra LifeSciences Corp. (NeuroSciences)...
The Issue: Lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.