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 10611080 of 53,829 recalls

Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience Kit Recalled by Medline Industries, LP Due to Firm received...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience Kits: DYNJ901048N ORTHO SPINE ST CLAIR DYNJ909123F UROLOGY MINOR...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia circuit kit Recalled by Medline Industries, LP Due to Firm...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
FoodOctober 9, 2025· Rong Shing Trading NY Inc

Recalled Item: Aojia Dried Red Bayberry Recalled by Rong Shing Trading NY Inc Due to...

The Issue: Product contains undeclared sulfites (7.39mg/serving) and cyclamates

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 9, 2025· Singh Trading Inc. DBA Roshni Foods

Recalled Item: Roshni Cinnamon Powder Recalled by Singh Trading Inc. DBA Roshni Foods Due...

The Issue: Product may contain elevated levels of lead and chromium.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2025· STAQ Pharma, Inc.

Recalled Item: Ketamine Hydrochloride Recalled by STAQ Pharma, Inc. Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
DrugOctober 9, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: N-nitroso-duloxetine impurity above the safety assessment...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2025· ibspot

Recalled Item: Taoscare Motion Sickness Patches 36-count box Recalled by ibspot Due to...

The Issue: Marketed Without an Approved NDA/ANDA

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2025· USV Private Limited

Recalled Item: Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 % Recalled by USV...

The Issue: Failed Impurities/Degradation Specifications: The result for 'Any individual...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2025· Amerisource Health Services LLC

Recalled Item: Sucralfate Tablets Recalled by Amerisource Health Services LLC Due to CGMP...

The Issue: CGMP Deviations: The recalling firm filed for Chapter 11 on September 30,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2025· STAQ Pharma, Inc.

Recalled Item: Hydromorphone HCL PF Recalled by STAQ Pharma, Inc. Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
DrugOctober 9, 2025· STAQ Pharma, Inc.

Recalled Item: FentaNYL Citrate PF Recalled by STAQ Pharma, Inc. Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 9, 2025· C-RAD POSITIONING AB

Recalled Item: Brand Name: Catalyst+ Product Name: Catalyst Recalled by C-RAD POSITIONING...

The Issue: Due to issues with the system's stereotactic radiosurgery (SRS) treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Myofunctional Research Company USA

Recalled Item: Myosa for Kids KS1 /Sp/Mb/Mp/Lb/Lc KS2 /Sc/Mb/Mc/Mp/Lb/Lc Myosa Recalled by...

The Issue: Due to firm mistakenly distributing product within the U.S. without FDA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Pivotal Health Solutions, Inc.

Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...

The Issue: The heat function may become damaged over time due to patients pressing on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Pivotal Health Solutions, Inc.

Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...

The Issue: The heat function may become damaged over time due to patients pressing on...

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

Class II — Potential Health HazardOngoing