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. 2,582 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,582 in last 12 months

Showing 32013220 of 47,764 recalls

Medical DeviceJanuary 15, 2025· TERRAGENE S.A.

Recalled Item: ASP BIOTRACE Auto Read 60 Steam BI Process Challenge Device Recalled by...

The Issue: Error in the IFU lists an incorrect incubation time on one occasion of 20...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2025· DeRoyal Industries Inc

Recalled Item: DeRoyal AMG Suction Connector Tubing Recalled by DeRoyal Industries Inc Due...

The Issue: The tubing may not ensure that the yankauer stays intact, and secure to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Single Use Guide Sheath Kits with the following product Recalled by...

The Issue: Potential for the radiopaque tip of the guide sheath component to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 15, 2025· Hologic, Inc

Recalled Item: Brand Name: Sertera Biopsy Device Product Name: Sertera Biopsy Device...

The Issue: Devices presented a condition in which the inner needle separated from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2025· Draeger Medical Systems, Inc.

Recalled Item: Infinity Central Station. Model Number: MS26800 The Infinity CentralStation...

The Issue: Edifier speakers (shipped in or after April 2023) may not annunciate when...

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

Class II — Potential Health HazardOngoing
FoodJanuary 13, 2025· Monkey Spit

Recalled Item: Monkey Spit "Atomic Mop" BBQ Sauce Recalled by Monkey Spit Due to Undeclared...

The Issue: Barbeque sauce product contains undeclared allergen listing of (Milk) in...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 13, 2025· Monkey Spit

Recalled Item: Monkey Spit "Monkey Mop" BBQ Sauce Recalled by Monkey Spit Due to Undeclared...

The Issue: Barbeque sauce product contains undeclared listing of (Milk) in product...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 13, 2025· Monkey Spit

Recalled Item: Monkey Spit "Swamp Mop" BBQ Sauce Recalled by Monkey Spit Due to Undeclared...

The Issue: Barbeque sauce product contains undeclared allergens (soy) contained in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 13, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by The Harvard Drug Group...

The Issue: CGMP Deviations: presence of Nitrosamine Drug Substances Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 B20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 B12 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Biplane Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 3 M15 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura CV20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 M20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 3 M12 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Biplane OR Table Recalled by PHILIPS MEDICAL SYSTEMS...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/15 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 5 M12 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing