Product Recalls in Hawaii

Product recalls affecting Hawaii — including food, drugs, consumer products, medical devices, and vehicles distributed to Hawaii. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,109 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
1,109 in last 12 months

Showing 601–620 of 27,645 recalls

Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Pollen Allergy Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: MPOX Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: GI Microbiome Profile Small Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Food Intolerance Test Large Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Neurotransmitters Plus Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Candida Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Adrenal Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Parasite Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Diabetes HbA1c Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: DHEA Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Herpes (HSV-1 & HSV-2) Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Candida Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Thyroid TSH Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Sperm Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Iron Deficiency Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Environmental Pollutants Profile Test Recalled by GET TESTED INTERNATIONAL...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software...

The Issue: A software timing and processor communication issue in MiniMed" 780G...

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 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 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