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. 2,544 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,544 in last 12 months

Showing 83018320 of 47,764 recalls

DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: SnoreStop Naso Spray Bulk Recalled by Homeocare Laboratories, Inc. Due to...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: Babelyn Diarrhea Drops Homeopathic Remedy Recalled by Homeocare...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: StellaLife VEGA Oral Care Gel Recalled by Homeocare Laboratories, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: Bebelyn Colic Drops Homeopathic Remedy Recalled by Homeocare Laboratories,...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: StellaLife VEGA Oral Care Spray Recalled by Homeocare Laboratories, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: StellaLife VEGA Oral Care Rinse Recalled by Homeocare Laboratories, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: DoloEar Earache Drops Recalled by Homeocare Laboratories, Inc. Due to cGMP...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: StellaLife VEGA Oral Care Gel Recalled by Homeocare Laboratories, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2023· Homeocare Laboratories, Inc.

Recalled Item: Kanjo Homeopathic Pain Relief Cream With Arnica Recalled by Homeocare...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 5, 2023· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Troponin I ES Reagent Pack Recalled by...

The Issue: Reagent packs could potentially contain incorrect wells, which will generate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2023· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Troponin I ES Calibrators Recalled by...

The Issue: Reagent packs could potentially contain incorrect wells, which will generate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2023· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: IABP may lose the ability to charge batteries in one or both bay slots....

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Select VA 21 with FD- A Mobile X-ray system Recalled by Siemens Medical...

The Issue: Incorrect glue was applied on the plexiglass sheet on the single tank cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2023· Datascope Corp.

Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: IABP may lose the ability to charge batteries in one or both bay slots....

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2023· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: An unexpected shutdown of the IABP may occur due to failures of tantalum...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2023· Datascope Corp.

Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: An unexpected shutdown of the IABP may occur due to failures of tantalum...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2023· B. Braun Medical, Inc.

Recalled Item: Design Options¿ / Epidural anesthesia kit (10 count carton) Recalled by B....

The Issue: Kits were assembled with the incorrect Filter Straw.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2023· Exactech, Inc.

Recalled Item: Exactech Ergo Impactor Handle Recalled by Exactech, Inc. Due to The ball and...

The Issue: The ball and spring housed within the locking mechanism of the handle can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2023· Luminex Corporation

Recalled Item: VERIGENE Clostridium difficile Nucleic Acid Test Recalled by Luminex...

The Issue: It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2023· Luminex Corporation

Recalled Item: Verigene Enteric Pathogens Nucleic Acid Test (EP) Recalled by Luminex...

The Issue: It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit...

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

Class II — Potential Health HazardOngoing