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. 1,077 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
1,077 in last 12 months

Showing 8821–8840 of 27,645 recalls

Medical DeviceSeptember 24, 2021· Philips Healthcare

Recalled Item: Philips Azurion systems with software releases 2.1(L1) and 2.1(L2) Recalled...

The Issue: 3D-RA is a reconstruction software product that can be used with the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2021· Implant Direct Sybron Manufacturing LLC

Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...

The Issue: Packaged dental implant contains a different size then the size declared on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2021· Implant Direct Sybron Manufacturing LLC

Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...

The Issue: Packaged dental implant contains a different size then the size declared on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2021· DiaSorin Molecular LLC

Recalled Item: SIMPLEXA COVID-19 Positive Control Pack Recalled by DiaSorin Molecular LLC...

The Issue: Due to unapproved raw materials used in the manufacturing of Covid-19...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2021· Medtronic Neuromodulation

Recalled Item: Clinician Programmer Application (CPA) model A610 Clinician Software...

The Issue: A software anomaly may occur with the clinician programmer application.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM SARS-CoV-2 Antigen Assay (100 Test Kit) Recalled by Siemens...

The Issue: Data provided in the Emergency Use Authorization (EUA) submission was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Z-Medica, LLC

Recalled Item: QuikClot Combat Gauze-For Temporary External Use To Control Traumatic...

The Issue: Lack of Packaging seal integrity may result in a sterile barrier breach.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· MEDTECH SAS

Recalled Item: ROSA One 3.1 Brain application The device is intended for Recalled by...

The Issue: The firm has become aware of a software anomaly affecting ROSA One 3.1 Brain...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 22, 2021· Philips Healthcare

Recalled Item: CombiDiagnost R90 is multi-functional general R/F systems. Recalled by...

The Issue: The Aleva monitor requires certain labels to be applied, some of which are...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Philips Healthcare

Recalled Item: ProxiDiagnost N90 is multi-functional general R/F systems. Recalled by...

The Issue: The Aleva monitor requires certain labels to be applied, some of which are...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur SARS-CoV-2 Antigen Assay (100 Test Kit) Recalled by Siemens...

The Issue: Data provided in the Emergency Use Authorization (EUA) submission was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· Philips Healthcare

Recalled Item: DigitalDiagnost C90 Recalled by Philips Healthcare Due to The Aleva monitor...

The Issue: The Aleva monitor requires certain labels to be applied, some of which are...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation/RayPlan versions 4 - 11A Recalled by RAYSEARCH LABORATORIES AB...

The Issue: An issue where the combined density in a dose grid voxel partially covered...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Estradiol II Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS RUB IgG (RBG) Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Lyme IgG II (LYM) Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS SARS-COV-2 IgM Recalled by bioMerieux, Inc. Due to bioMerieux has been...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS PRG Progesterone Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2021· bioMerieux, Inc.

Recalled Item: VIDAS Measles IgG (MSG) Recalled by bioMerieux, Inc. Due to bioMerieux has...

The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...

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

Class II — Potential Health HazardOngoing