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. 1,109 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
1,109 in last 12 months

Showing 1041–1060 of 47,764 recalls

Medical DeviceOctober 9, 2025· Myofunctional Research Company USA

Recalled Item: Myosa for Kids KS1 /Sp/Mb/Mp/Lb/Lc KS2 /Sc/Mb/Mc/Mp/Lb/Lc Myosa Recalled by...

The Issue: Due to firm mistakenly distributing product within the U.S. without FDA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· C-RAD POSITIONING AB

Recalled Item: Brand Name: Catalyst+ Product Name: Catalyst Recalled by C-RAD POSITIONING...

The Issue: Due to issues with the system's stereotactic radiosurgery (SRS) treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Controller (Standalone)...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate II¿ Controller (standalone)...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: Ultrasound System 1300 Recalled by B-K Medical A/S Due to GE HealthCare has...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: bk5000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Pivotal Health Solutions, Inc.

Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...

The Issue: The heat function may become damaged over time due to patients pressing on...

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

Class II — Potential Health HazardOngoing
DrugOctober 8, 2025· ASTRAZENECA PHARMACEUTICALS

Recalled Item: Fasenra (benralizumab) Injection Recalled by ASTRAZENECA PHARMACEUTICALS Due...

The Issue: Lack of Assurance of Sterility:

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 8, 2025· Cellavision AB

Recalled Item: or BS737162 Automated Digital Cell Morphology analyzer DI-60 Recalled by...

The Issue: Automated cell-locating device barcode reader may read the barcode of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Lithotriptor Recalled by Olympus Corporation of the Americas Due...

The Issue: The device may either fail to start up, or the transducer may start briefly...

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

Class II — Potential Health HazardOngoing
DrugOctober 8, 2025· Mohamed Hagar

Recalled Item: Mojo Max Fusion XXX Recalled by Mohamed Hagar Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 7, 2025· Rising Pharma Holding, Inc.

Recalled Item: Carbidopa Recalled by Rising Pharma Holding, Inc. Due to Product mix up:...

The Issue: Product mix up: complaint received that sealed medication bottle contained...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...

The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...

The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2025· Trividia Health, Inc.

Recalled Item: Good Neighbor Pharmacy Recalled by Trividia Health, Inc. Due to...

The Issue: Manufacturing defect causing LCD display issues with missing or partial...

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

Class II — Potential Health HazardOngoing
DrugOctober 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...

The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2025· NeuroLogica Corporation

Recalled Item: GM85 Digital Mobile X-ray imaging System Recalled by NeuroLogica Corporation...

The Issue: The four (4) M5 bolts that secure the Tube Head Unit to the end of the arm...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2025· Philips Respironics, Inc.

Recalled Item: SimplyGo Mini Recalled by Philips Respironics, Inc. Due to Certain serial...

The Issue: Certain serial numbers of the SimplyGo Mini standard battery kit contain a...

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

Class II — Potential Health HazardOngoing
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
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