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.

53,829 total recalls
1,161 in last 12 months

Showing 1541–1560 of 53,829 recalls

Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Fresenius Medical Care Holdings, Inc.

Recalled Item: Optiflux¿ High Flux E-beam Dialyzer Model Numbers: (1) 0500316E OPTIFLUX...

The Issue: To provide further information to the user to ensure proper use of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK System Paclitaxel Set Recalled by Baxter Healthcare Corporation...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK System Non_DEHP Extenstion Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Getinge Disinfection Ab

Recalled Item: Getinge 88-Series Washer- Disinfector. Model Number: 88-5. Recalled by...

The Issue: Potential for device to overheat during operation if the circulation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CONTINU-FLO Solution Set Recalled by Baxter Healthcare Corporation Due to IV...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2025· Baxter Healthcare Corporation

Recalled Item: CLEARLINK SYSTEM EXTENSION SET Recalled by Baxter Healthcare Corporation Due...

The Issue: IV sets may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2025· Vantive US Healthcare LLC

Recalled Item: Sharesource Connectivity Platform for Use with Homechoice Claria Product...

The Issue: Vantive has identified a software defect within the Sharesource Claria...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: BIOGRAPH One (DE). Model Number: 11689172. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396 Recalled by...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Verio Dot. Model Number: 10684333. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra fit. Model Number: 10849580. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Cima.X (DE). Model Number: 11647158. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
DrugAugust 28, 2025· Granules Pharmaceuticals Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217. Recalled by Siemens...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
DrugAugust 28, 2025· Granules Pharmaceuticals Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:

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

Class III — Low RiskOngoing
Refund
DrugAugust 28, 2025· Granules Pharmaceuticals Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:

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

Class III — Low RiskOngoing
Refund