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. 1,891 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,891 in last 12 months

Showing 2854128560 of 53,829 recalls

Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: T5-NT Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: T10-NT Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Intera 0.5T Standard Recalled by Philips Electronics North America...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: T5 Model 78104 Product Usage: Indicated for use as a Recalled by Philips...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: ACS-NT Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Panorama 1.0T Recalled by Philips Electronics North America Corporation Due...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Healthcare Lunar: a) DPX NT Recalled by GE Medical Systems Ultrasound &...

The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Healthcare: a) Prodigy Recalled by GE Medical Systems Ultrasound &...

The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns TCM II Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Update to cooler-heater cleaning instructions.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Ingenia 1.5T CX Recalled by Philips Electronics North America Corporation...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Healthcare Lunar: a) DPX Duo Recalled by GE Medical Systems Ultrasound &...

The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Intera 1.5T Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Nobel Biocare Usa Llc

Recalled Item: Nobel Biocare 17¿ Multi-Unit Abutment Recalled by Nobel Biocare Usa Llc Due...

The Issue: The product label has missing information, such as the lot number and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo HX2 Temperature Management System Recalled by Terumo Cardiovascular...

The Issue: Update to cooler-heater cleaning instructions.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Intera 1.0T Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Achieva 1.5T: 1) Nova (Dual) Recalled by Philips Electronics North America...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
FoodMarch 16, 2018· Smucker Natural Foods, Inc.

Recalled Item: SANTA CRUZ organic BLACKBERRY POMEGRANATE fruit spread NET WT 9.5 Recalled...

The Issue: The firm was notified that the product did not have an ingredient panel or...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMarch 16, 2018· Smucker Natural Foods, Inc.

Recalled Item: SANTA CRUZ organic SEEDLESS RED RASPBERRY fruit spread NET WT Recalled by...

The Issue: The firm was notified that the product did not have an ingredient panel or...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund