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 3416134180 of 53,829 recalls

DrugNovember 14, 2016· Akorn Inc

Recalled Item: Desoximetasone Ointment USP Recalled by Akorn Inc Due to Failed Stability...

The Issue: Failed Stability Specifications; out-of specification value for homogeneity...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 13, 2016· Ultimate Body Tox

Recalled Item: Ultimate Body Tox PRO capsules Recalled by Ultimate Body Tox Due to...

The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 12, 2016· KRAFT HEINZ FOODS COMPANY

Recalled Item: Weight Watchers Smart Ones Recalled by KRAFT HEINZ FOODS COMPANY Due to...

The Issue: Possible contamination of product with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT 728326 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 728231 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 728321 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 728323 Recalled by Philips Medical Systems (Cleveland)...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 728232 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
FoodNovember 11, 2016· House Of Flavors, Inc.

Recalled Item: Ashby's Sterling Peanut Butter Landslide Ice Cream Recalled by House Of...

The Issue: House of Flavors, Inc. is voluntarily recalling a limited portion of Ashby's...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2016· First Source, LLC

Recalled Item: Wegmans Milk Chocolate Covered Pretzels Recalled by First Source, LLC Due to...

The Issue: Milk Chocolate covered pretzels have incorrect rear label. The rear label is...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...

The Issue: Lack of 510k clearance for design modification.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...

The Issue: Lack of 510k clearance for design modification.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...

The Issue: An increase in reports indicating that the reprocessed H12LP Trocar...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2016· OraSure Technologies, Inc.

Recalled Item: Barbiturates Intercept Micro-Plate EIA (enzyme immunoassay Recalled by...

The Issue: Shipping error. Cocaine metabolite Microplate distributed instead of...

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

Class III — Low RiskOngoing
DrugNovember 9, 2016· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: bulk solution tested...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2016· Sandoz Inc

Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2016· Sandoz Inc

Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 9, 2016· Seth Ellis Chocolatier, LLC

Recalled Item: Free2b Sun Cups Chocolate. Made With SunButter Sunflower Spread. Packaged...

The Issue: Free2b Foods recalled the Sun Cups Chocolate due to potential contamination...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 9, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: GAM Kirschner Wire Recalled by Stryker Howmedica Osteonics Corp. Due to A...

The Issue: A review of packaging revealed the seal integrity of the pouch may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 4.0 Recalled by RAYSEARCH LABORATORIES AB Due to Software...

The Issue: Software anomaly; an issue was found with the proton Pencil Beam Scanning...

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

Class II — Potential Health HazardOngoing