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. 999 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
999 in last 12 months

Showing 37741–37760 of 53,829 recalls

Medical DeviceFebruary 5, 2016· Beckman Coulter Inc.

Recalled Item: Allegra X-5 rotor yoke Recalled by Beckman Coulter Inc. Due to A defective...

The Issue: A defective rotor yoke on Allegra X-5 allows improper rotor seating on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64:Computed Tomography X-ray Systems Recalled by Philips Medical...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP Computed Tomography X-ray Systems Recalled by Philips...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Volcano Corporation

Recalled Item: Volcano R100 Sterile Equipment Cover Recalled by Volcano Corporation Due to...

The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Computed Tomography X-ray Systems Recalled by Philips Medical...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray Systems Recalled by Philips Medical...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray Systems Recalled by Philips...

The Issue: The firm was notified of a software error in which the system may not...

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

Class II — Potential Health HazardOngoing
FoodFebruary 5, 2016· Living Tree Community Foods

Recalled Item: Living Tree Community Foods Organic Macadamia Nuts Recalled by Living Tree...

The Issue: Recall of macadamia nuts and macadamia butter after notification by...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2016· Living Tree Community Foods

Recalled Item: Living Tree Community Foods Organic Macadamia Butter Recalled by Living Tree...

The Issue: Recall of macadamia nuts and macadamia butter after notification by...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Dried Sticks Hot under the following Recalled by...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Smoked Pepperoni under the following labels:...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Goetburg Summer Sausage under the following...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Dried Sausage Sticks under the following...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Summer Sausage under the following labels:...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 4, 2016· The Sausage Maker, Inc.

Recalled Item: THE SAUSAGE MAKER SEASONING Trail Bologna under the following labels:...

The Issue: Fermento ingredient contains undeclared whey protein and skim milk powder

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 4, 2016· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Perfusion Tubing Pack Recalled by Medtronic Perfusion...

The Issue: Medtronic is notifying customers who have or may receive specific lots of...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 4, 2016· Draeger Medical, Inc.

Recalled Item: Evita Infinity V500 Ventilator Recalled by Draeger Medical, Inc. Due to The...

The Issue: The battery capacity of the optional PS500 power supply unit for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: (Stryker) AccuPlace Straight Level Needle Guide Recalled by Stryker...

The Issue: During an evaluation of the product packaging, it was determined that there...

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

Class II — Potential Health HazardOngoing