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 45414560 of 47,764 recalls

Medical DeviceAugust 6, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion 7M20 systems with FlexArm ceiling-mounted system Recalled by...

The Issue: The motorized longitudinal movement of the FlexArm stand may be inconsistent...

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

Class II — Potential Health HazardOngoing
DrugAugust 5, 2024· Zeco LLC

Recalled Item: Rubbing Alcohol (70% Isopropyl Alcohol) Recalled by Zeco LLC Due to CGMP...

The Issue: CGMP Deviations: sterile water not used for production

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2024· Zeco LLC

Recalled Item: HAND-I-SAN Recalled by Zeco LLC Due to CGMP Deviations: sterile water not...

The Issue: CGMP Deviations: sterile water not used for production

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 5, 2024· QUANTUM SURGICAL SAS

Recalled Item: The EPIONE device v1.0.2 is a user controlled Recalled by QUANTUM SURGICAL...

The Issue: Quantum Surgical has become aware that a component (central axis) inside the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· MICROVENTION INC.

Recalled Item: ERIC Retrieval Device ER174030 ER176044 The ERIC Retrieval Recalled by...

The Issue: Due to Retrieval Device product labels stating the incorrect expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: ImpellaCP SmartAssistSetAPAC Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Pump 371 Set Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 SmartAssist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Pump 381 Pump Set (US) Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set APAC Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Impella CP Pump Set Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing