Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,367 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,367 in last 12 months

Showing 2798128000 of 48,219 recalls

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 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· 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· 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
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· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Protein 1 Control H 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· 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· 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 22, 2017· Zimmer Biomet, Inc.

Recalled Item: ECT Internal Fracture Fixation Drill 2.5 mm Diameter (.098 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: ECT Internal Fracture Fixation Drill Bits 3.2 mm Diameter (.126 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: Zimmer Periarticular Locking Plate System Locking Screw Tap Standard...

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: M/DN Intramedullary Fixation Distal Drill Pilot Tip 3.2 mm Diameter Recalled...

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: 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: 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· Exactech, Inc.

Recalled Item: Exactech 1.5" Novation Calcar Planer Guide Tip To assist the Recalled by...

The Issue: The firm determined that the labeling (surgical technique) should be updated...

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

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

Recalled Item: PROMETRA II Programmable Infusion Pump Recalled by Flowonix Medical, Inc....

The Issue: Flowonix Medical received a report of a patient implanted with the Prometra...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Natus Medical Incorporated

Recalled Item: The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended...

The Issue: Olympic Pasteurmatic 3000/3500 Systems are recalled because they do not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Sentinel CH SPA

Recalled Item: MULTIGENT Creatinine (Enzymatic) Recalled by Sentinel CH SPA Due to Reagent...

The Issue: Reagent 1 component may result in Quality Control values shifting out of...

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 4.5 mm Diameter 145 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