Product Recalls in West Virginia

Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,336 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,336 in last 12 months

Showing 3340133420 of 48,376 recalls

Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...

The Issue: If images are sent without an order in the system, they will be matched with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Merge PACS (Picture Archiving Communication System) is...

The Issue: Cut lines on the image may present horizontally rather than vertically.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Becton Dickinson & Co.

Recalled Item: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) Recalled by Becton...

The Issue: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2016· Becton Dickinson & Company

Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...

The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2016· Becton Dickinson & Company

Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...

The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2016· Intuitive Surgical, Inc.

Recalled Item: EndoWrist Stapler 45 and Stapler 30 instruments used on the Recalled by...

The Issue: Potential for unexpected motion of the Xi Stapler jaws on the da Vinci Xi...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2016· Monteris Medical Corp

Recalled Item: NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe Recalled by...

The Issue: Monteris received a report that the sapphire lens on a 2.2SF probe fractured...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2016· Hansen Medical Inc

Recalled Item: Magellan Robotic Catheter Accessory Kits Recalled by Hansen Medical Inc Due...

The Issue: Firm's quarterly dose audit testing showed that one batch was radiated below...

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

Class II — Potential Health HazardOngoing
DrugMarch 25, 2016· B. Braun Medical Inc

Recalled Item: 5% Dextrose Injection USP Recalled by B. Braun Medical Inc Due to...

The Issue: Non-Sterility: fungal contamination due to leaking containers.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 25, 2016· Bryant Ranch Prepack Inc.

Recalled Item: Venlafaxine 75 mg Tablet Recalled by Bryant Ranch Prepack Inc. Due to...

The Issue: Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine...

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2016· AbbVie Inc.

Recalled Item: Zemplar (paricalcitol) capsules Recalled by AbbVie Inc. Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2016· Lupin Limited

Recalled Item: Escitalopram Tablets USP 20 mg Recalled by Lupin Limited Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16 Computed Tomography X-ray systems is intended to produce...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Radiology Computed Tomography X-ray systems Recalled by...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems is intended to Recalled...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Dimension Vista 1500 Intelligent Lab System running on software versions...

The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Oncology Computed Tomography X-ray systems Recalled by...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Abbott Laboratories

Recalled Item: CELL-DYN Emerald Cleaner Recalled by Abbott Laboratories Due to Three lots...

The Issue: Three lots of CELL-DYN Emerald Cleaner may have occurrences where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 16 Power Computed Tomography X-ray systems is intended...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· CareFusion 303, Inc.

Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to The Alaris PC units...

The Issue: The Alaris PC units model 8015 may display a system error code 133.6080 due...

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

Class II — Potential Health HazardOngoing