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. 2,404 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,404 in last 12 months

Showing 2280122820 of 27,462 recalls

Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Richard-Allan Scientific Bio-Tite Specimen Containers. Product Usage: 10%...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Boston Scientific CRM Corp

Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to...

The Issue: Boston Scientific identified a subset of COGNISTM CRT-Ds and TELIGENTM ICDs...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Richard-Allan Scientific Specimen Transportation System. Product Usage: 10%...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Boston Scientific CRM Corp

Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...

The Issue: Boston Scientific identified a subset of COGNISTM CRT-Ds and TELIGENTM ICDs...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2014· Richard-Allan Scientific Company

Recalled Item: Cardinal Health Prefilled Buffered 10% Formalin. Product Usage:10% NBF is...

The Issue: The affected lots could have NBF concentrations that are lower or higher...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer used in conjunction with the da Recalled by...

The Issue: Intuitive Surgical is initiating a voluntary correction relating to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Multi-Function Electrodes (MFE) Part Number: 8900-4012...

The Issue: Product sterility is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2014· Baxter Healthcare Corp

Recalled Item: Baxter 2B8013 Empty INTRA VIA Container with PVC Ports (Sterile Recalled by...

The Issue: Particulate matter found inside the fluid path.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes with 10-ft (3 m)...

The Issue: Product sterility is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Multi-Function Electrodes (MFE) Single. Part number:...

The Issue: Product sterility is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2014· Baxter Healthcare Corp

Recalled Item: Baxter 2B8011 Empty INTRA VIA Container with PVC Ports Recalled by Baxter...

The Issue: Particulate matter found inside the fluid path.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes with 10-ft (3 m)...

The Issue: Product sterility is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿¿ Systems HBc Total (HBcT) Kit. For In Vitro Recalled by...

The Issue: Increased imprecision and positive bias is observed with patient samples and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur¿ Systems HBc Total (HBcT) Recalled by Siemens...

The Issue: Increased imprecision and positive bias is observed with patient samples and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman EDS 3 Drainage System with Ventricular Catheter (External Drainage...

The Issue: tubing within the system that drains CSF may leak or disconnect from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman EDS 3 Drainage System (no Ventricular Catheter) (External Drainage...

The Issue: tubing within the system that drains CSF may leak or disconnect from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Lumbar Drainage Catheter Kit II with EDS 3 (External Recalled by...

The Issue: tubing within the system that drains CSF may leak or disconnect from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Primus Medical LLC

Recalled Item: AC Powered adjustable bed frame. AC powered adjustable bed frame Recalled by...

The Issue: Firm received several complaints that the head deck actuator bracket had...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2014· Invivo Corporation

Recalled Item: Philips Expression Information Portal (IP5) Model 865471. The IP5 is...

The Issue: Frozen Display Numerics and Disabled Menu Keys after extended run time. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2014· Eyemart Express Ltd

Recalled Item: Prescription eyeglass safety lenses. Vision correction Recalled by Eyemart...

The Issue: Prescription eyeglass safety lenses did not meet specifications.

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

Class II — Potential Health HazardOngoing