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. 2,849 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,849 in last 12 months

Showing 961980 of 53,829 recalls

Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Telemetry Transmitter Model/Catalog Number:...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iX10...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: elite...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM8...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number:...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Central Monitoring System Model/Catalog...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: X8...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Fetal & Maternal Monitor Model/Catalog...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM50...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Edan Diagnostics

Recalled Item: Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM20...

The Issue: As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA...

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

Class II — Potential Health HazardOngoing
FoodOctober 24, 2025· Water Pure, Inc.

Recalled Item: My Bladder Recalled by Water Pure, Inc. Due to Potential E. coli Contamination

The Issue: Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 24, 2025· E.A. Sween Co.

Recalled Item: Deli Express BBQ Pulled Pork on a sesame bun. Net Recalled by E.A. Sween Co....

The Issue: Potential foreign material (plastic)

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2025· Cipla USA, Inc.

Recalled Item: Lanthanum Carbonate chewable tablets Recalled by Cipla USA, Inc. Due to...

The Issue: Failed stability specifications: Out of specification for hardness test

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2025· Cipla USA, Inc.

Recalled Item: Lanthanum Carbonate chewable tablets Recalled by Cipla USA, Inc. Due to...

The Issue: Failed stability specifications: Out of specification for hardness test

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 24, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAMMOMAT Inspiration Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: There were instances where the operator table was sold together with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAMMOMAT Fusion Recalled by Siemens Medical Solutions USA, Inc Due to There...

The Issue: There were instances where the operator table was sold together with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAMMOMAT Revelation Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: There were instances where the operator table was sold together with a...

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

Class II — Potential Health HazardOngoing
DrugOctober 23, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Bromocriptine Mesylate Capsules Recalled by Zydus Pharmaceuticals (USA) Inc...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund