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. 1,921 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,921 in last 12 months

Showing 2496124980 of 53,829 recalls

DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2019· Valeant Pharmaceuticals North America LLC

Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...

The Issue: Failed Dissolution Specifications: high out of specification results for...

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

Class III — Low RiskOngoing
Refund
FoodJanuary 30, 2019· 1908 Brands

Recalled Item: Bundle Organics Bar Salty Nuts and Seeds Recalled by 1908 Brands Due to...

The Issue: Bundle Organics snack bars are recalled due to the presence of mold.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 30, 2019· 1908 Brands

Recalled Item: Bundle Organics Bar Oatmeal Raisin Recalled by 1908 Brands Due to Bundle...

The Issue: Bundle Organics snack bars are recalled due to the presence of mold.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 30, 2019· 1908 Brands

Recalled Item: Bundle Organics Bar Chocolate-Maca Recalled by 1908 Brands Due to Bundle...

The Issue: Bundle Organics snack bars are recalled due to the presence of mold.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 30, 2019· 1908 Brands

Recalled Item: Bundle Organics Bar Carrot Walnut Recalled by 1908 Brands Due to Bundle...

The Issue: Bundle Organics snack bars are recalled due to the presence of mold.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 30, 2019· 1908 Brands

Recalled Item: Bundle Organics Bar Chocolate Chip Recalled by 1908 Brands Due to Bundle...

The Issue: Bundle Organics snack bars are recalled due to the presence of mold.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 30, 2019· 1908 Brands

Recalled Item: Bundle Organics Bar Goji-Berry Cashew Recalled by 1908 Brands Due to Bundle...

The Issue: Bundle Organics snack bars are recalled due to the presence of mold.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 30, 2019· U&I CORP.

Recalled Item: Velofix SA cervical cage Recalled by U&I CORP. Due to The vertical...

The Issue: The vertical dimensions of screw-hole position in some standalone cages...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2019· Matrix Surgical Holdings, LLC

Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Left - Product Usage: Recalled...

The Issue: Product mislabeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2019· Matrix Surgical Holdings, LLC

Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Right - Product Usage: Recalled...

The Issue: Product mislabeling.

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

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2019· US Compounding Inc

Recalled Item: Ephedrine Sulfate Recalled by US Compounding Inc Due to Lack of assurance of...

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 29, 2019· COLLINS AEROSPACE

Recalled Item: TASE 400 Imaging systems Recalled by COLLINS AEROSPACE Due to the Nominal...

The Issue: the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2019· COLLINS AEROSPACE

Recalled Item: TASE 500 Imaging systems Recalled by COLLINS AEROSPACE Due to the Nominal...

The Issue: the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb...

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

Class II — Potential Health HazardOngoing
DrugJanuary 28, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Bimatoprost Ophthalmic Solution 0.03% Recalled by Lupin Pharmaceuticals Inc....

The Issue: Failed Impurities/Degradation Specifications: OOS results observed in any...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 28, 2019· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON NX2 Elite Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: The action is being initiated due to internal testing which identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2019· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON NX3 Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: The action is being initiated due to internal testing which identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2019· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON NX3 Elite Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: The action is being initiated due to internal testing which identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2019· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON NX2 Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: The action is being initiated due to internal testing which identified a...

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

Class II — Potential Health HazardOngoing