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. 1,044 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,044 in last 12 months

Showing 24301–24320 of 53,829 recalls

Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge- BEQ-T 9411 Lurie Children's 1/4 ADAPT Material:709000485R01...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-TOP 26402 ECC PACK Material: 701062310 Recalled by Maquet...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge- BEQ-TOP 37200 E-Circuit Bioline Heparin Material:...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge BEQ-TOP 38300 ADULT CPS QID Material:701055862R01 Recalled by...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-TOP 3700 Tubing Pack Material: 701049510 Recalled by...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-TOP 8013 ECC QUADROX iD Pack RF32 Material: 701047962...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-TOP 38002 ADULT SPECIALTY Material: Recalled by Maquet...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-TOP 38900 ECC PACK Material: 701056368 Recalled by Maquet...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1) Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing