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

53,829 total recalls
922 in last 12 months

Showing 50501–50520 of 53,829 recalls

DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Verapamil Injection Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Dexamethasone PF Recalled by Pallimed Solutions Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: DMSO Aqueous Irrigation 50% Recalled by Pallimed Solutions Due to Lack of...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Atropine Injection Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Testosterone Cypionate/Testosterone Enanthate Injection Recalled by Pallimed...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Diazepam Injectable Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: MIC with B6 and B12 Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2013· Pallimed Solutions

Recalled Item: Methylcobalamin PF Recalled by Pallimed Solutions Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; FDA inspectional findings resulted in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2013· Watson Laboratories, Inc.-(Actavis) - Florida

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by Watson...

The Issue: Failed Tablet/Capsule Specifications: Broken tablets

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2013· Actavis Inc

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Broken tablets

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2013· Actavis South Atlantic LLC

Recalled Item: buPROPion Hydrochloride Extended-Release Tablets (XL) 300 mg Recalled by...

The Issue: Failed USP Dissolution Test Requirements: Out-of-specification dissolution...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 22, 2013· Lighthouse For The Blind

Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...

The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...

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

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2013· Lighthouse For The Blind

Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...

The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...

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

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD ONE VIOLET AND ONE BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC)...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· Advanced Sterilization Products

Recalled Item: EVOTECH Endoscope Cleaner & Reprocessor System Recalled by Advanced...

The Issue: Advanced Sterilization Products (ASP) has determined that a limited number...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC) Recalled by DePuy...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...

The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 200 Sterilization System Recalled by Advanced Sterilization Products...

The Issue: The recall was initiated because Advanced Sterilization Products (ASP) has...

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

Class II — Potential Health HazardOngoing