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. 1,047 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,047 in last 12 months

Showing 19061–19080 of 53,829 recalls

FoodAugust 5, 2020· The Kroger Co

Recalled Item: AFIN JARLSBERG CHEESE SPREAD KIT in plastic tubs Recalled by The Kroger Co...

The Issue: Potential contamination with Salmonella Newport.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 5, 2020· The Kroger Co

Recalled Item: MURRAY'S SOUTHWESTERN JARLSBERG DIP in plastic tubs Recalled by The Kroger...

The Issue: Potential contamination with Salmonella Newport.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 5, 2020· The Kroger Co

Recalled Item: MURRAY'S CHADS SMOKED GOUDA DIP in plastic tubs Recalled by The Kroger Co...

The Issue: Potential contamination with Salmonella Newport.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 5, 2020· The Kroger Co

Recalled Item: DELI RANCH CHEESE SPREAD KIT in plastic tubs Recalled by The Kroger Co Due...

The Issue: Potential contamination with Salmonella Newport.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 5, 2020· The Kroger Co

Recalled Item: MURRAY'S JALEPENO JARLSBERG DIP in plastic tubs Recalled by The Kroger Co...

The Issue: Potential contamination with Salmonella Newport.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 5, 2020· The Kroger Co

Recalled Item: DELI JARLSBERG DIP in plastic tubs Recalled by The Kroger Co Due to...

The Issue: Potential contamination with Salmonella Newport.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 5, 2020· The Kroger Co

Recalled Item: JARLSBERG DIP in plastic tubs Recalled by The Kroger Co Due to Potential...

The Issue: Potential contamination with Salmonella Newport.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 5, 2020· The Kroger Co

Recalled Item: DELI SOUTHWEST CHEESE SPREAD KIT in plastic tubs Recalled by The Kroger Co...

The Issue: Potential contamination with Salmonella Newport.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 5, 2020· The Kroger Co

Recalled Item: DELI JARLSBERG JALAPENO DIP in plastic tubs Recalled by The Kroger Co Due to...

The Issue: Potential contamination with Salmonella Newport.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: PC Unit Front Case with Keypad Replacement Kits: TC10008389 ASSY Recalled by...

The Issue: The pump module keypad may exhibit keys that are unresponsive or stuck as a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· Integra LifeSciences Corp.

Recalled Item: Integra Padgett Dermatome Set - Product Usage: are intended for Recalled by...

The Issue: lntegra LifeSciences has identified through a number of complaints that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· Integra LifeSciences Corp.

Recalled Item: Integra Padgett Electric Dermatome Set - Product Usage: are intended...

The Issue: lntegra LifeSciences has identified through a number of complaints that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: BD Alaris System Recalled by CareFusion 303, Inc. Due to The Alaris PC unit...

The Issue: The Alaris PC unit can display incorrect syringe type and/or syringe sizes....

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: Alaris System PC Unit Model 8015 Recalled by CareFusion 303, Inc. Due to The...

The Issue: The pump module keypad may exhibit keys that are unresponsive or stuck as a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: BD Alaris System. The EtCO2 module is a capnograph indicated for continuous...

The Issue: Infusion pump component defect may result in interruption of patient monitoring

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· Hologic, Inc

Recalled Item: Panther Fusion Tube Tray Recalled by Hologic, Inc Due to Tube trays may leak...

The Issue: Tube trays may leak which could invalidate patient results or assay...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: BD Alaris System PC Unit Model 8100 (Pump Module) and Recalled by CareFusion...

The Issue: Pump Module keypad may exhibit keys that are unresponsive or stuck as a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· Integra LifeSciences Corp.

Recalled Item: 13 ft Handpiece Cable Recalled by Integra LifeSciences Corp. Due to lntegra...

The Issue: lntegra LifeSciences has identified through a number of complaints that the...

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

Class II — Potential Health HazardOngoing
DrugAugust 4, 2020· Eosera, Inc.

Recalled Item: Ear Pain MD Pain Relief Drops with 4% Lidocaine (lidocaine Recalled by...

The Issue: cGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2020· Eosera, Inc.

Recalled Item: Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%) 0.5 FL OZ (15 mL) bottles...

The Issue: cGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund