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

53,829 total recalls
953 in last 12 months

Showing 48281–48300 of 53,829 recalls

DrugSeptember 11, 2013· Physicians Total Care, Inc.

Recalled Item: Loratadine 24 HR-OTC Recalled by Physicians Total Care, Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Affected lot numbers may contain...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 10, 2013· Wexford Labs Inc

Recalled Item: Ready to Use Thymo-Cide Recalled by Wexford Labs Inc Due to Expired active...

The Issue: Expired active ingredient was used in the manufacture of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Steris Corporation

Recalled Item: VERIFY¿ Dual Species Self-Contained Biological Indicator Recalled by Steris...

The Issue: STERIS has identified that the population of the G. stearothermophilus...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Integra Limited

Recalled Item: Brand Names: Integra¿ Camino 110-4 Intracranial Pressure (ICP) Monitoring...

The Issue: Integra LifeSciences has identified through an internal evaluation that in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Aesculap, Inc.

Recalled Item: Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar...

The Issue: Complaints were received for the GN161 Bipolar Foot Control reporting that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Baxter Healthcare Corp.

Recalled Item: Dual Luer Lock Cap The device is intended for use Recalled by Baxter...

The Issue: The firm is recalling lots 10043 and 10044 due to loose particulate matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Smiths Medical Recalled by Smiths Medical ASD, Inc. Due to Smiths Medical is...

The Issue: Smiths Medical is conducting a voluntary recall of PORT-A-CATH¿ and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Smith Medical Recalled by Smiths Medical ASD, Inc. Due to Smiths Medical is...

The Issue: Smiths Medical is conducting a voluntary recall of PORT-A-CATH¿ and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Hospira Inc.

Recalled Item: Hospira RECEPTAL LINERS: 1L(1000mL) Recalled by Hospira Inc. Due to Hospira...

The Issue: Hospira has become aware of customers using the incorrect size Receptal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2013· Hospira Inc.

Recalled Item: Hospira RECEPTAL CANISTERS: 1L(1000mL) Recalled by Hospira Inc. Due to...

The Issue: Hospira has become aware of customers using the incorrect size Receptal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: 14951-48 Recalled by Hospira Inc. Due to...

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: List No. 14220-28 Recalled by Hospira Inc....

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: List No. 14212-28 Recalled by Hospira Inc....

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: 19683-28 Recalled by Hospira Inc. Due to...

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: 19734-28 Recalled by Hospira Inc. Due to...

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
DrugSeptember 9, 2013· Avella of Deer Valley, Inc.

Recalled Item: Bevacizumab 1.25 mg/0.05 mL PF Recalled by Avella of Deer Valley, Inc. Due...

The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 9, 2013· Avella of Deer Valley, Inc.

Recalled Item: Vancomycin PF (BSS) 1% Recalled by Avella of Deer Valley, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Ofloxacin Ophthalmic Solution Recalled by PACK Pharmaceuticals, LLC Due to...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund