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. 2,582 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,582 in last 12 months

Showing 10611080 of 47,764 recalls

DrugOctober 6, 2025· Heritage Pharmaceuticals Inc

Recalled Item: Desipramine Hydrochloride Tablets Recalled by Heritage Pharmaceuticals Inc...

The Issue: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2025· Heritage Pharmaceuticals Inc

Recalled Item: Desipramine Hydrochloride Tablets Recalled by Heritage Pharmaceuticals Inc...

The Issue: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2025· Heritage Pharmaceuticals Inc

Recalled Item: Desipramine Hydrochloride Tablets Recalled by Heritage Pharmaceuticals Inc...

The Issue: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2025· Heritage Pharmaceuticals Inc

Recalled Item: Desipramine Hydrochloride Tablets Recalled by Heritage Pharmaceuticals Inc...

The Issue: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2025· VIONA PHARMACEUTICALS INC

Recalled Item: Tavaborole Topical solution 5% Recalled by VIONA PHARMACEUTICALS INC Due to...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 6, 2025· POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC

Recalled Item: OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control...

The Issue: A labeling error was identified on the affected product. The expiration date...

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

Class III — Low RiskOngoing
Medical DeviceOctober 6, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Food Panel 3 Specific Allergen Recalled by Siemens Healthcare Diagnostics,...

The Issue: The barcode orientation on affected devices causes incorrect scanning order...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400...

The Issue: Sterility compromised from small holes that may occur during packaging of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: 3gAllergy Specific IgE Universal Kit Recalled by Siemens Healthcare...

The Issue: The barcode orientation on affected devices causes incorrect scanning order...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Oak Mix Specific Allergen Recalled by Siemens Healthcare...

The Issue: The barcode orientation on affected devices causes incorrect scanning order...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Single Use Electrosurgical Snare SD-400 Product Name:...

The Issue: Sterility compromised from small holes that may occur during packaging of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Tandem Diabetes Care, Inc.

Recalled Item: Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are...

The Issue: Insulin pump includes a vibration motor that gives tactile feedback for any...

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

Class I — Serious Health HazardOngoing
FoodOctober 3, 2025· New York Mutual Trading, Inc.

Recalled Item: Frozen Crab Paste Recalled by New York Mutual Trading, Inc. Due to...

The Issue: Undeclared allergen ingredients (fish, soy, and wheat)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 3, 2025· Medtronic Perfusion Systems

Recalled Item: MC3 VitalFlow Console Recalled by Medtronic Perfusion Systems Due to As of...

The Issue: As of August 6, 2025, Medtronic has received eleven reports of VitalFlow...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: TruDi¿ Navigation System - Multi Instrument Adapter Recalled by Integra...

The Issue: It was determined that when the navigation system is configured with...

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

Class II — Potential Health HazardOngoing