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 49614980 of 27,645 recalls

Medical DeviceDecember 7, 2023· Philips North America

Recalled Item: Incisive CT Recalled by Philips North America Due to If the Patient...

The Issue: If the Patient Interface Monitor (PIM) Cable is plugged/unplugged frequently...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Stryker, Inc.

Recalled Item: Stryker Neurovascular Recalled by Stryker, Inc. Due to The microcatheter IFU...

The Issue: The microcatheter IFU contains an intended use that has not been evaluated...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Stryker, Inc.

Recalled Item: Stryker Neurovascular Recalled by Stryker, Inc. Due to The microcatheter IFU...

The Issue: The microcatheter IFU contains an intended use that has not been evaluated...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Flo-Thru Intraluminal Shunt Recalled by Baxter Healthcare Corporation...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Floseal Hemostatic Matrix Fast Prep Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Vascu-Guard Peripheral Vascular Patch (US) Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter FloSeal Hemostatic Matrix NL Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Flo-Rester Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: PERI-GUARD SUPPLE Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Coseal Premix Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Vascu-Guard Peripheral Vascular Patch (GLOBAL) Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Preveleak Surgical Sealant Recalled by Baxter Healthcare Corporation...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Ostene Hemostasis Material Recalled by Baxter Healthcare Corporation...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Vascular Probe Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter FloSeal Hemostatic Matrix RECOTHROM Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Abiomed, Inc.

Recalled Item: Impella Connect Recalled by Abiomed, Inc. Due to The following features have...

The Issue: The following features have been disabled from the web-based portal because...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2023· Oakworks Inc

Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...

The Issue: Backrest platform stress fracture - the table is not operational in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2023· Oakworks Inc

Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...

The Issue: Backrest platform stress fracture - the table is not operational in an...

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

Class II — Potential Health HazardOngoing