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 52215240 of 27,645 recalls

Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Oscor Intro Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Axillary Insertion Introducer -Introducer(s) are intended for...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Oscor Introducer Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Luminex Corporation

Recalled Item: Luminex VERIGENE BC-GP Utility Tray (5-Pack Carrier) Recalled by Luminex...

The Issue: Potentially defective utility trays in the reagent kits.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Introducer Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Oscor Introducer Kit Recalled by Abiomed, Inc. Due to Hole(s) to the...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· GE Hangwei Medical Systems, Co. LTD

Recalled Item: The System is designed as a modular system with components Recalled by GE...

The Issue: GE HealthCare has become aware of the potential that incorrect torque has...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed KIT Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· GE Hangwei Medical Systems, Co. LTD

Recalled Item: The System is designed as a modular system with components Recalled by GE...

The Issue: GE HealthCare has become aware of the potential that incorrect torque has...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· APN Health LLC

Recalled Item: Navik 3D v2 Recalled by APN Health LLC Due to IFU update

The Issue: IFU update

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

Class III — Low RiskOngoing
Medical DeviceNovember 6, 2023· Merit Medical Systems, Inc.

Recalled Item: Merit Maestro Microcatheter Recalled by Merit Medical Systems, Inc. Due to...

The Issue: The sterility of microcatheter and infusion system devices cannot be guaranteed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus ENDOEYE HD II Rigid Videoscope Catalog Numbers: WA50040A Recalled by...

The Issue: Reports of a pink or green coloration of the image. If the issue is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2023· Maquet Medical Systems USA

Recalled Item: CARDIOHELP-i Heart Lung Support System- A blood oxygenation and carbon...

The Issue: Certain factory settings for the device were incorrectly described in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2023· Nurse Assist, LLC

Recalled Item: Sterile Water/Saline: Brand Name: Product Name/Product Code: CARDINAL: 100ML...

The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2023· Merit Medical Systems, Inc.

Recalled Item: Merit Pursue Microcatheter Recalled by Merit Medical Systems, Inc. Due to...

The Issue: The sterility of microcatheter and infusion system devices cannot be guaranteed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2023· Sarnova HC, Llc

Recalled Item: Curaplex Field Cric Kit with ET Tube Recalled by Sarnova HC, Llc Due to It...

The Issue: It was determined that the Endotracheal Tube Holder included in certain kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2023· Sarnova HC, Llc

Recalled Item: Curaplex Cricothyrotomy Field Kit with Instruments Recalled by Sarnova HC,...

The Issue: It was determined that the Endotracheal Tube Holder included in certain kits...

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

Class II — Potential Health HazardOngoing