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. 2,378 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,378 in last 12 months

Showing 2574125760 of 27,462 recalls

Medical DeviceFebruary 20, 2013· Orthopedic Alliance LLC

Recalled Item: Bipolar Cap Recalled by Orthopedic Alliance LLC Due to The recall of the...

The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2013· Spinal Solutions, LLC

Recalled Item: 40 mm Rod Recalled by Spinal Solutions, LLC Due to The recall of the Loaner...

The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2013· Spinal Solutions, LLC

Recalled Item: 60 mm Rod Recalled by Spinal Solutions, LLC Due to The recall of the Loaner...

The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2013· Genesys Orthopedic Systems, LLC

Recalled Item: 3.75mm x 12mm Fixed Cervical Screws. Components of the Genesys Recalled by...

The Issue: Manufacturing residue may be present on the cervical screws. Use of this...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2013· Spinal Solutions, LLC

Recalled Item: 14 x 11 x 6mm 7 deg 14 x 11 Recalled by Spinal Solutions, LLC Due to The...

The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2013· Spinal Solutions, LLC

Recalled Item: Fang Screw 20mm Fang Plate 21mm Product Usage: Spinal Solutions Recalled by...

The Issue: The recall of the Loaner Bin and Sterilization Trays for implants and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2013· Tecan US, Inc.

Recalled Item: Tecan Freedom EVO with Touch Tools Suite Version 3.0 The Recalled by Tecan...

The Issue: WIth TouchTools 3.0 after the execution of a Rich User Prompt in Display and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2013· Remel Inc

Recalled Item: Remel X/pect Flu A&B Control Swabs Recalled by Remel Inc Due to Flu A+...

The Issue: Flu A+ Control Swabs incorrectly give Flu A- results when used for quality...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 19, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic DPL Single Stage Venous Cannula with Metal Tip Recalled by...

The Issue: Potential for uncharacteristically rough metal edges to occur along the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2013· Hospira Inc.

Recalled Item: Minibore Extension Set Recalled by Hospira Inc. Due to Hospira, Inc. is...

The Issue: Hospira, Inc. is voluntarily recalling one lot of list 14699-28, Minibore...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Ge Healthcare It

Recalled Item: Imagecast PACS with Centricity RIS-IC versions prior to 10.6 Update Recalled...

The Issue: A software defect was discovered that causes images to be out of context...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· GE Healthcare

Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...

The Issue: Using Merge Exam in single Study Mode may result in Missing Study Record...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Ge Medical Systems Information T

Recalled Item: Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging...

The Issue: It was reported from a complaint that study category labels of "Prior" and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 Compact computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 60 computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2013· Biomerieux Inc

Recalled Item: VITEK 2 XL computer system when equipped with the following Recalled by...

The Issue: There is a potential to link an isolate result to the wrong patient and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2013· Moller Vital

Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...

The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 and Ingenuity Computed Tomography X-Ray Systems The Brilliance...

The Issue: This field change order is being released to update software and customer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX Micros IM2 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...

The Issue: Horiba Medical is recalling ABX Micros IM2 Data Management System because it...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 15, 2013· Moller Vital

Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...

The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...

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

Class II — Potential Health HazardOngoing