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. 1,768 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,768 in last 12 months

Showing 5014150160 of 53,829 recalls

Medical DeviceApril 15, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Hand Switch - Electric Pen Drive Recalled by Synthes USA HQ, Inc....

The Issue: Synthes received a complaint from a customer in which the Hand Switch for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Medrad Inc

Recalled Item: DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris Recalled by...

The Issue: The firm is recalling these power cables due to a latent design reliability...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle InsuLinx Blood Glucose Monitoring System: For In Vitro Diagnostic...

The Issue: AT rare, extremely high glucose levels (1024 mg/dL and above), the FreeStyle...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 15, 2013· Hill-Rom, Inc.

Recalled Item: Hill-Rom 1000 Bed Recalled by Hill-Rom, Inc. Due to Complaints have been...

The Issue: Complaints have been reported for brakes disengaging when the bed is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray systems Product Usage: The Brilliance CT 64...

The Issue: Philips Healthcare received reports from the field that certain Brilliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2013· Cypress Medical Products LLC

Recalled Item: Cypress Medical Products LLC Recalled by Cypress Medical Products LLC Due to...

The Issue: Cypress Medical Products LLC is voluntarily recalling one lot of the Owens...

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

Class II — Potential Health HazardOngoing
DrugApril 15, 2013· NuVision Pharmacy, Inc.

Recalled Item: HCG (Lyophilized) Stock # 21714 Recalled by NuVision Pharmacy, Inc. Due to...

The Issue: Lack of Assurance of Sterility: The recall is being initiated due to a lack...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2013· Apothecure, Inc

Recalled Item: The firm is recalling all lots of sterile products compounded Recalled by...

The Issue: Lack of Assurance of Sterility: The recall is being initiated due to the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2013· NuVision Pharmacy, Inc.

Recalled Item: Sermorelin/GHRP-6 Recalled by NuVision Pharmacy, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The recall is being initiated due to a lack...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 12, 2013· OPMX, LLC

Recalled Item: Pentrexcilina Jarabe NF (dextromethorphan HBr and guaifenesin) liquid...

The Issue: Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 12, 2013· OPMX, LLC

Recalled Item: Pentrexcilina (acetaminophen Recalled by OPMX, LLC Due to Labeling: Not...

The Issue: Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 12, 2013· Coloplast Manufacturing US, LLC

Recalled Item: Rostorelle L Recalled by Coloplast Manufacturing US, LLC Due to Mislabeling

The Issue: Coloplast is recalling one lot of Restorelle L prosthesis because it is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Ethicon Endo-Surgery Inc

Recalled Item: LIGACLIP¿ Endoscopic Rotating Multiple Clip Applier Convenience Kit (Flex...

The Issue: Ethicon Endo-Surgery is initiating a voluntary recall for LIGACLIP¿ 10mm M/L...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Becton Dickinson & Co.

Recalled Item: BBL DrySlide PYR Kit Recalled by Becton Dickinson & Co. Due to In-vitro...

The Issue: In-vitro diagnostic agents were placed into incorrect packaging for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2013· Progressive Medical Inc

Recalled Item: Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes -...

The Issue: Product coatings require 510K approval.

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

Class II — Potential Health HazardOngoing