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. 2,314 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,314 in last 12 months

Showing 821840 of 48,219 recalls

DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: Wecare Calasoothe Recalled by Blossom Pharmaceuticals Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: WeCare Recalled by Blossom Pharmaceuticals Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP20. Product Number: M8001A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
DrugOctober 31, 2025· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: 3% Polocaine DENTAL Recalled by Novocol Pharmaceutical of Canada, Inc. Due...

The Issue: Defective container: cracked/broken cartridges

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: 2% Xylocaine DENTAL with Epinephrine 1:100 Recalled by Novocol...

The Issue: Defective container: cracked/broken cartridges

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: Globe Clotrimazole Cream Recalled by Blossom Pharmaceuticals Due to cGMP...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: OraVerse Recalled by Novocol Pharmaceutical of Canada, Inc. Due to Defective...

The Issue: Defective container: cracked/broken cartridges

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: Nivagen Recalled by Blossom Pharmaceuticals Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Cipla Limited

Recalled Item: Phytonadione Injectable Emulsion Recalled by Cipla Limited Due to Failed...

The Issue: Failed Stability Specifications: Observed OOS results: eg results for colour...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: Lanashield Skin Barrier Recalled by Blossom Pharmaceuticals Due to cGMP...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: Wecare Enema Recalled by Blossom Pharmaceuticals Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: Dynashield Recalled by Blossom Pharmaceuticals Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: Nivagen Recalled by Blossom Pharmaceuticals Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: Dynagel Recalled by Blossom Pharmaceuticals Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2025· Philips Ultrasound, LLC

Recalled Item: Lumify Diagnostic Ultrasound System models : 795005 Recalled by Philips...

The Issue: Ultrasound system compatibility issues with Apple devices running iOS 18 may...

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

Class II — Potential Health HazardOngoing
DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: Globe Clotrimazole Cream USP Recalled by Blossom Pharmaceuticals Due to cGMP...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP30. Product Number: M8002A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP2. Product Number: M8102A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP90. Product Number: M8010A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker MV3 bariatric bed Recalled by Stryker Medical Division of Stryker...

The Issue: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX...

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

Class II — Potential Health HazardOngoing