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. 1,757 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,757 in last 12 months

Showing 3200132020 of 48,219 recalls

Medical DeviceMay 19, 2016· Implant Direct Sybron Manufacturing, LLC

Recalled Item: 6534-08N InterActive¿ Implant Open-Tray Transfer Narrow Part Number:...

The Issue: The incorrect sized product, InterActive Implant Open-Tray Transfer Wide,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Kalare DREX-KL80 X-ray generator Recalled by Toshiba American...

The Issue: It was discovered that the generator of the system could possibly terminate...

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

Class II — Potential Health HazardOngoing
FoodMay 19, 2016· The Kroger Co

Recalled Item: Kroger SALTED SUNFLOWER KERNELS 6 oz (170g) INGREDIENTS: SUNFLOWER KERNELS...

The Issue: The firm was notified by their supplier that they are expanding their recall...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 19, 2016· The Kroger Co

Recalled Item: Kroger SALAD TOPPERS Roasted & Salted Sunflower Kernels NET WT Recalled by...

The Issue: The firm was notified by their supplier that they are expanding their recall...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugMay 19, 2016· West-Ward Columbus Inc

Recalled Item: Oxycodone HCl Recalled by West-Ward Columbus Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specification; 9 month stability

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

Class III — Low RiskOngoing
Refund
DrugMay 19, 2016· Galderma Laboratories, L.P.

Recalled Item: Doxycycline Recalled by Galderma Laboratories, L.P. Due to Labeling:...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: Some expiries and lot...

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

Class III — Low RiskOngoing
Refund
DrugMay 18, 2016· Teva North America

Recalled Item: Divalproex Sodium Delayed-release Tablets USP Recalled by Teva North America...

The Issue: Failed Tablet/Capsule Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Pediatric ThermoGard¿ Dual Dispersive Electrodes (for patients 5-15 kg.)...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Adult Dual Dispersive Electrodes (for patients >15 kg.) Recalled by Conmed...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Pediatric Dual Dispersive Electrodes (for patients 5-15 kg.) Recalled by...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Elekta, Inc.

Recalled Item: Monaco RTP System Product Usage: The Monaco system is used Recalled by...

The Issue: When DICOM exporting a 3D Monaco plan and the "Composite Field Sequencing"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics (OCD) confirmed a potential for biased calcium...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2016· Conmed Corporation

Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...

The Issue: A version of the dual dispersive electrodes may not be compatible with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard ventilator- Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: TCA Board Recalled by Carefusion 211 Inc dba Carefusion Due to CareFusion...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA GDE/UIM upgrade kit Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: Gas Delivery Engine (GDE)-1st Generation Recalled by Carefusion 211 Inc dba...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard with Compressor ventilator- Recalled by Carefusion 211 Inc dba...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 17, 2016· Carefusion 211 Inc dba Carefusion

Recalled Item: AVEA Standard with Compressor ventilator Recalled by Carefusion 211 Inc dba...

The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...

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

Class I — Serious Health HazardOngoing