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. 2,562 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,562 in last 12 months

Showing 861880 of 48,770 recalls

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
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX700. Product Number: 865241. 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 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 Patient Monitor MX850. Product Number: 866470. 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 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 MP50. Product Number: M8004A. 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 MP80. Product Number: M8008A. 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 MX100. Product Number: 867033. 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 MP40. Product Number: M8003A. 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· Aizu Olympus Co., Ltd.

Recalled Item: Olympus OER-Elite Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...

The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...

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 Multi Measurement Server X2. Product Number: M3002A. 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 MP60. Product Number: M8005A. 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 MP5. Product Number: M8105A. 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 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· 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
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX400. Product Number: 866060. 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 Multi-Measurement Module X3. Product Number: 867030. 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· Aizu Olympus Co., Ltd.

Recalled Item: Olympus OER-Pro Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...

The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...

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 MX550. Product Number: 866066. 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 Patient Monitor MX750. Product Number: 866471. 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