Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,272 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,272 in last 12 months

Showing 841860 of 48,770 recalls

DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: Dynashield Skin Protectant 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: Globe Zinc Oxide Ointment USP Zinc Oxide 20% Skin Protectant Recalled by...

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 Pharmaceuticals 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: 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: 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
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX800. Product Number: 865240. Recalled by...

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: Cook-Walte Recalled by Novocol Pharmaceutical of Canada, Inc. Due to...

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: Lidocaine HCI 2% and Epinephrine 1:100 Recalled by Novocol Pharmaceutical of...

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· 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
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 Patient Monitor MX600. Product Number: 865242. Recalled by...

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· 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
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 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· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX500. Product Number: 866064. Recalled by...

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 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
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
Medical DeviceOctober 31, 2025· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker Arise 1000EX mattress Recalled by Stryker Medical Division of...

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