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. 1,800 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,800 in last 12 months

Showing 2804128060 of 48,219 recalls

Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Drill Bit Quick-Connect 3-Fluted 4.5 mm Diameter 195 mm Length 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 Fixation Drill Bits 2.5 mm Diameter (0.98 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: Zimmer Periarticular Locking Plate System Recalled by Zimmer Biomet, Inc....

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 1.5 mm Diameter 70 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: M/DN Intramedullary Fixation Femoral Drill 3.7 mm Diameter Replaces...

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 12.5...

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: Drill Bit Quick-Connect 3.2 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
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Zimmer Periarticular Locking Plate System Drill Standard 2.7 mm Diameter...

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: Zimmer Periarticular Locking Plate System Cannulated Drill 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: Herbert Cannulated Bone Screw System Recalled by Zimmer Biomet, Inc. Due to...

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
DrugMay 22, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications: out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications: out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications: out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications: out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund
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· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima CT580 Recalled by GE Healthcare, LLC Due to It was...

The Issue: It was discovered that an issue has been identified that can result in a...

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
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery IQ X-ray system Recalled by GE Healthcare, LLC Due...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing