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. 1,009 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,009 in last 12 months

Showing 33681–33700 of 53,829 recalls

Medical DeviceDecember 27, 2016· Villa Sistemi Medicali S.P.A.

Recalled Item: Juno DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...

The Issue: Patient fell from the table because the footrest of the device detached from...

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· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell...

The Issue: Patient fell from the table because the footrest of the device detached from...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2016· Villa Sistemi Medicali S.P.A.

Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...

The Issue: Patient fell from the table because the footrest of the device detached from...

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

Class II — Potential Health HazardOngoing
DrugDecember 27, 2016· The Harvard Drug Group

Recalled Item: Aripiprazole Tablets Recalled by The Harvard Drug Group Due to Superpotent...

The Issue: Superpotent Drug; out of specification results for assay (manufacturer)

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

Class III — Low RiskOngoing
Refund
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 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
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 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 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· 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 22, 2016· AGFA Healthcare Corp.

Recalled Item: IMPAX Cardiovascular The IMPAX CV Reporting module consists of a Recalled by...

The Issue: A customer experienced when using IMPAX CV Reporting software, specifically,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2016· Mako Surgical Corporation

Recalled Item: MAKO RIO THA Application User Guides Recalled by Mako Surgical Corporation...

The Issue: Five (5) AFMEA Risk Control Measures are missing from the MAKO RIO THA...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2016· Tosoh Smd Inc

Recalled Item: Keyspan High-High Speed USB to Serial Adapter Product Usage: The Recalled by...

The Issue: Power outages causes reporting software to shutdown.

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

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

Recalled Item: Dan Dee - Sour Cream & Onion Flavored Potato Chips sold in 7/8 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
FoodDecember 22, 2016· Bickel's Snack Foods Inc

Recalled Item: Seyfert-Sour Cream & Onion Flavored Potato Chips sold in 2 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: Cabana- Sour Cream & Onion Flavored Potato Chips sold in 5 oz. bags 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