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. 1,850 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,850 in last 12 months

Showing 3368133700 of 53,829 recalls

Medical DeviceDecember 27, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC 9900 Elite. MDL Numbers: D148942 Recalled by GE OEC Medical Systems, Inc...

The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC 9800...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· GE OEC Medical Systems, Inc

Recalled Item: OEC 9800. MDL Numbers: D222250 Recalled by GE OEC Medical Systems, Inc Due...

The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC 9800...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Philips Electronics North America Corporation

Recalled Item: Philips Cisco 3850 layer 3 switch Recalled by Philips Electronics North...

The Issue: May experience a loss of centralized monitoring.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Endologix

Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...

The Issue: Endologix updated the Instructions for Use (IFU) and implemented...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Endologix

Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...

The Issue: Endologix updated the Instructions for Use (IFU) and implemented...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number...

The Issue: Maquet has received 3 confirmed complaints related to the Li-lon Battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Express Dry Seal Suction OASIS DRAIN Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Atrium Medical Corporation

Recalled Item: Maquet Express Dry Seal Suction Chest Drain Recalled by Atrium Medical...

The Issue: Chest drains manual vent valve located at the top of affected chest drains...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2016· Elekta, Inc.

Recalled Item: Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation...

The Issue: Cross profile for Varian 60 degree wedge shows "horns."

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

Class II — Potential Health HazardOngoing
DrugDecember 22, 2016· Aurobindo Pharma USA Inc

Recalled Item: Venlafaxine Hydrochloride extended release capsules Recalled by Aurobindo...

The Issue: Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2016· Roxane Laboratories, Inc.

Recalled Item: Furosemide Tablets USP Recalled by Roxane Laboratories, Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: An unusually thick tablet was reported...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2016· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: TEMAZEPAM CAPSULES USP Recalled by Vintage Pharmaceuticals LLC, DBA...

The Issue: Failed Stability Specifications

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

Class III — Low RiskOngoing
Refund
FoodDecember 22, 2016· Schreiber Food International

Recalled Item: Ambrosia Quality Foods Brand 4/1 gallon Worcestershire Sauce Net 128 Fl. Oz....

The Issue: Ambrosia brand 4/1 Gallon Worcestershire Sauce may contain undeclared peanuts.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 22, 2016· Bickel's Snack Foods Inc

Recalled Item: Bon Ton-Sour Cream & Onion Flavored Potato Chips sold in 2.75 oz Recalled by...

The Issue: Bickel's Snack Foods, Inc. of York, PA is voluntarily recalling all snack...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 22, 2016· Bickel's Snack Foods Inc

Recalled Item: Bickel's Sour Cream & Onion Flavored Potato Chips sold in .75 oz. Recalled...

The Issue: Bickel's Snack Foods, Inc. of York, PA is voluntarily recalling all snack...

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

Class I — Serious Health HazardOngoing
Refund