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. 2,566 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,566 in last 12 months

Showing 37813800 of 27,645 recalls

Medical DeviceMay 17, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade Recalled...

The Issue: Cranial Caudal Blades manufactured incorrectly could result in fracture...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade Recalled...

The Issue: Cranial Caudal Blades manufactured incorrectly could result in fracture...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System Recalled by...

The Issue: Potential for there to be a fluid ingress into the handle of the harvesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Siemens Healthcare Diagnostics Inc

Recalled Item: Software version 5.3 in: RAPIDPoint 500e Blood Gas System (USA) Recalled by...

The Issue: Siemens Healthineers has identified an issue with the RAPIDPoint500e system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Biomet, Inc.

Recalled Item: RingLoc Bi-Polar Hip System Acetabular Cup Recalled by Biomet, Inc. Due to...

The Issue: 41 mm acetabular outer heads were potentially assembled with a 42 mm locking...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for...

The Issue: Potential for there to be a fluid ingress into the handle of the harvesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· B Braun Medical Inc

Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...

The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· B Braun Medical Inc

Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...

The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· B Braun Medical Inc

Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...

The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2024· B Braun Medical Inc

Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...

The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Medtronic Perfusion Systems

Recalled Item: TourniKwik Tourniquet Set (CFN 79012) Recalled by Medtronic Perfusion...

The Issue: Incorrect component placed in four manufactured lots of the TourniKwik"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE FILMARRAY Gastrointestinal (GI) Panel (30 test kit) Recalled by...

The Issue: Due to increase of false positive Vibrio/Vibrio Cholerae results when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim XR 5 Implantable Pulse Generator Recalled by Abbott Medical...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim 5 Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim 7 Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim XR 7 Implantable Pulse Generator Recalled by Abbott Medical...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim Plus 7 Implantable Pulse Generator Recalled by Abbott...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim Plus 5 Implantable Pulse Generator Recalled by Abbott...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim DRG Implantable Pulse Generator Recalled by Abbott Medical...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim Plus 5 Implantable Pulse Generator Recalled by Abbott...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing