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

47,764 total recalls
2,562 in last 12 months

Showing 46614680 of 27,645 recalls

Medical DeviceJanuary 30, 2024· Applied Medical Resources Corp

Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...

The Issue: Their is the potential that Universal Clip applier may not load clip after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Applied Medical Resources Corp

Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...

The Issue: Their is the potential that Universal Clip applier may not load clip after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 SS/PD Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO Recalled by Angiodynamics,...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 15 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2024· SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION

Recalled Item: Shimadzu Recalled by SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Due to...

The Issue: Due to capacitor manufacturing issue, their is a potential that Flat Panel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Embrace Drill Tower Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due...

The Issue: The surgical techniques for the Embrace Shoulder Instruments -Drill Tower...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2024· Canon Medical System, USA, INC.

Recalled Item: MRI system: Vantage Elan Recalled by Canon Medical System, USA, INC. Due to...

The Issue: For some MRI systems, it has been found that some of the maximum Spatial...

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

Class II — Potential Health HazardOngoing