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. 1,898 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,898 in last 12 months

Showing 2746127480 of 53,829 recalls

FoodJuly 12, 2018· The Pictsweet Company

Recalled Item: Pictsweet Farms Steam'ables Baby Brussels Sprouts***NET WT 12 OZ...

The Issue: Undeclared allergens on the labeling.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 11, 2018· Spacelabs Healthcare, Ltd.

Recalled Item: Arkon Anesthesia Delivery System with Arkon Software Version 2.70 Recalled...

The Issue: Arkon Anesthesia Delivery System may go into a failed state (mechanical...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: P400 PREM U/M 16FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: P400 PREM U/M 18FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides failed to meet current claims for Limit of Blank (LoB), Limit of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CREA Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides did not meet the current claims for Limit of Blank (LoB), Limit...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: TEMP SENSE SILICONE 14FR5CC2W Recalled by COVIDIEN LLC Due to The...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...

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

Class III — Low RiskOngoing
DrugJuly 11, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to Failed...

The Issue: Failed Stability Specifications: lot out of specification for elevated water...

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

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to...

The Issue: Superpotent Drug: lots out of specification for elevated sodium chloride and...

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

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to...

The Issue: Superpotent Drug and Failed Stability Specifications: lot out of...

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

Class III — Low RiskOngoing
Refund
DrugJuly 10, 2018· Valeant Pharmaceuticals North America LLC

Recalled Item: Diazepam Rectal Gel Recalled by Valeant Pharmaceuticals North America LLC...

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

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 10, 2018· Arrow International Inc

Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...

The Issue: The packaging may not be sealed. If the packaging is compromised in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2018· Arrow International Inc

Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...

The Issue: The packaging may not be sealed. If the packaging is compromised in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2018· Merit Medical Systems, Inc.

Recalled Item: ChloraPrep With Tint Recalled by Merit Medical Systems, Inc. Due to A...

The Issue: A nonsterile bulk product designated for further processing in a tray was...

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

Class II — Potential Health HazardOngoing
DrugJuly 9, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Triamterene and Hydrochlorothiazide Tablets Recalled by Mylan...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund