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. 2,364 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,364 in last 12 months

Showing 3152131540 of 48,219 recalls

Medical DeviceJuly 12, 2016· Resmed Corporation

Recalled Item: Quattro Air FFM MED  AMER Recalled by Resmed Corporation Due to Masks in...

The Issue: Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2016· Mckesson Medical Imaging Group

Recalled Item: McKesson Radiology Recalled by Mckesson Medical Imaging Group Due to The...

The Issue: The STAT priority icon was not displayed in the Study List when the study...

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

Class II — Potential Health HazardOngoing
DrugJuly 12, 2016· Supernus Pharmaceuticals, Inc.

Recalled Item: Trokendi XR (topiramate) extended-release capsule Recalled by Supernus...

The Issue: Superpotent Drug: Failure of assay specifications in the capsule.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 12, 2016· ELITech Group B.V.

Recalled Item: Viva-ProE Systems Recalled by ELITech Group B.V. Due to Software...

The Issue: Software malfunction; The action being taken due to the device becoming...

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

Class III — Low RiskOngoing
FoodJuly 12, 2016· McCain Foods USA

Recalled Item: Breaded stuffed Jalapenos poppers labeled in part: Anchor breaded Fiesta...

The Issue: Firm used Flour from General Mills that has been contaminated with E. Coli O121.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2016· McCain Foods USA

Recalled Item: Fire roasted Poblano & Jalapeno popper bites packaged in a Recalled by...

The Issue: Firm used Flour from General Mills that has been contaminated with E. Coli O121.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2016· HVL, LLC

Recalled Item: METABOLIC CLEASNSE VEG 1151 grams Recalled by HVL, LLC Due to Product...

The Issue: Product labeling does not declare milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2016· HVL, LLC

Recalled Item: ULTRA PROTEIN VANILLA¿ 948 grams Recalled by HVL, LLC Due to Product...

The Issue: Product labeling does not declare milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 11, 2016· HVL, LLC

Recalled Item: METABOLIC CLEANSE REVISED 1181 grams Recalled by HVL, LLC Due to Product...

The Issue: Product labeling does not declare milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2016· Actavis Inc

Recalled Item: Dextroamphetamine Sulfate Extended-Release Capsules Recalled by Actavis Inc...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: INRatio Prothrombin Time (PT) Monitoring System Model Number: 0100007...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR Test Strips Model Number: 0100071 Recalled by Alere San...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Testing System Model Number: 0200431...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 Replacement Monitor (Home) Model Number: 0200457 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Trinity Biotech Captia Measles IgM Recalled by Clark Laboratories, Inc....

The Issue: The product lot failed to meet QC acceptance criteria during stability...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Monitoring System Model Number: 55128A...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio Replacement Monitor Model Number: 0100137 Usage: The INRatio...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR System Professional Model Numbers: 0100004 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio/ INRatio2 PT/INR Test Strips Model Number: 99007EU Recalled by...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· American National Mfg Inc

Recalled Item: Panacea Air Pro Mattress Control Unit Recalled by American National Mfg Inc...

The Issue: The Panacea Air Pro Mattress Control Unit is being recalled due to a...

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

Class II — Potential Health HazardOngoing