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 2804128060 of 48,219 recalls

Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: ECT Internal Fracture Fixation Quick-Connect Drill 3.5 mm Diameter 11 cm...

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 Quick-Connect Drill 2.5 mm Diameter 11 cm...

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 2.5 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 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: 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 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: 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: 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: 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 Natural Nail System Freehand Drill 4.3 mm Diameter 152.5 mm Length...

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 1.5 mm Diameter (.059 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· 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· 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· 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
DrugMay 19, 2017· DYNAMIC TECHNICAL FORMULATIONS

Recalled Item: Biotech Underground Tri-Ton Hardcore Formula capsules Recalled by DYNAMIC...

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 19, 2017· Neusoft Medical Systems Co., Ltd.

Recalled Item: Neusoft Medical NeuViz 64 Multi-slice CT Scanner System Recalled by Neusoft...

The Issue: Software defect

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· Neusoft Medical Systems Co., Ltd.

Recalled Item: Neusoft NeuViz 128 Multi-slice CT Scanner System Product Usage: The Recalled...

The Issue: Software defect

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· Fisher Diagnostics

Recalled Item: Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30...

The Issue: An issue was discovered with the Pacific Hemostasis Fibrinogen Degradation...

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

Class II — Potential Health HazardOngoing