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. 1,010 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,010 in last 12 months

Showing 31501–31520 of 53,829 recalls

Medical DeviceMay 23, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Protein 1 Control Recalled by Siemens Healthcare...

The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare and LeadCare II test Kits. Product Usage:...

The Issue: Underestimates the lead concentration of venous blood samples when the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 23, 2017· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare Ultra and LeadCare Plus test Kits. Product...

The Issue: Underestimates the lead concentration of venous blood samples when the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 23, 2017· Pentax of America Inc

Recalled Item: Ultrasound Video Gastroscope Recalled by Pentax of America Inc Due to Error...

The Issue: Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Shimadzu Medical Systems Usa Com

Recalled Item: SHIMADZU RADspeed Pro Catalog Number: RADspeed Pro Recalled by Shimadzu...

The Issue: Cracks may occur over time on the tube holding shaft near the base of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Shimadzu Medical Systems Usa Com

Recalled Item: SHIMADZU FDR Visionary Catalog Number: FDR Visionary Suite Stationary x-ray...

The Issue: Cracks may occur over time on the tube holding shaft near the base of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Shimadzu Medical Systems Usa Com

Recalled Item: SHIMADZU Ceiling Type X-ray Tube Support CH-200/CH-200M Catalog Number:...

The Issue: Cracks may occur over time on the tube holding shaft near the base of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Protein 1 Control M Recalled by Siemens Healthcare...

The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...

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

Class II — Potential Health HazardOngoing
FoodMay 23, 2017· MusclMasster, LLC

Recalled Item: The Green Herb 100% Natural AL-ER-G Recalled by MusclMasster, LLC Due to...

The Issue: MusclMasster, LLC is recalling all bottles of Al-Er-G Capsules because they...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 23, 2017· The Kroger Co

Recalled Item: Kroger Dessert Cups yellow sponge cakes NET WT 6.5 oz Recalled by The Kroger...

The Issue: The firm was notified that the product does not list MILK in the allergen...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: ECT Internal Fracture Fixation Drill Bits 1.5 mm Diameter (.059 Inch)...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Drill Bit Quick-Connect 2.0 mm Diameter 100 mm Length Recalled by Zimmer...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: ECT Internal Fracture Fixation Drill 2.7 mm Diameter (.106 Inch) Recalled by...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Drill Bit Quick-Connect 1.5 mm Diameter 85 mm Length Recalled by Zimmer...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: ECT Internal Fracture Fixation Drill 3.5 mm Diameter (.138 Inch) Recalled by...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Straight Shank Drill Bit 4.0 mm Diameter Recalled by Zimmer Biomet, Inc. Due...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: NCB Periprosthetic Plate System Drill Bit With Quick-Coupling 3.5 mm...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: ECT Internal Fracture Fixation Drill 4.5 mm Diameter (.177 Inch) Recalled by...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Drill Bit Jacobs Chuck 2.0 mm Diameter 85 mm Length Recalled by Zimmer...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Drill Bit Quick-Connect 3.2 mm Diameter 195 mm Length Recalled by Zimmer...

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

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

Class II — Potential Health HazardOngoing