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 641660 of 47,764 recalls

Medical DeviceNovember 21, 2025· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Emphasizing instructions for LVP duration programming located in the IFU.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2025· Medline Industries, LP

Recalled Item: Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK Recalled...

The Issue: Firm received multiple complaints regarding tubing disconnecting from oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2025· Roche Diagnostics Operations, Inc.

Recalled Item: The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay...

The Issue: Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator...

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

Class II — Potential Health HazardOngoing
DrugNovember 20, 2025· Fagron Compounding Services

Recalled Item: Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical...

The Issue: Incorrect Product Formulation

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 20, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2025· Medtronic Neuromodulation

Recalled Item: Restore Clinician Programmer Application (CP App) Recalled by Medtronic...

The Issue: Software issue where a Device Reset message displayed on the app was unable...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2025· Steris Corporation

Recalled Item: AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product...

The Issue: Wire connected to the electrical box may shift out of its intended position,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2025· Steris Corporation

Recalled Item: AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product...

The Issue: Wire connected to the electrical box may shift out of its intended position,...

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

Class II — Potential Health HazardOngoing
DrugNovember 18, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Nebivolol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 18, 2025· AGFA Healthcare Corp.

Recalled Item: Brand name: AGFA Digital Radiography X- Ray system DR 800 Recalled by AGFA...

The Issue: It is possible to exceed the maximum allowed Air Kerma rate (AKR) of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2025· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Hardware configuration of the BeneVision Central Monitoring System (CMS)...

The Issue: When the Worstation of the BeneVision DMS has a specific hardware...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number:...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· ETAC A/S

Recalled Item: Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers:...

The Issue: A customer experienced that during assembly and load testing of the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· Sophysa

Recalled Item: The Pressio 2 ICP Monitoring System Recalled by Sophysa Due to Customer...

The Issue: Customer complaints of Pressio monitor rebooting.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2025· Sheathing Technologies Inc

Recalled Item: Sheathes3D Seamless Viral Barrier Recalled by Sheathing Technologies Inc Due...

The Issue: Vaginal/rectal ultrasound probe covers with a viral barrier may have product...

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

Class II — Potential Health HazardOngoing
FoodNovember 16, 2025· Prime Food Processing LLC.

Recalled Item: Lava Bun with Salted Egg Yolk orange packaging (Frozen) Unsalted Recalled by...

The Issue: Products do not declare milk in the Contains statement or the ingredient...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 16, 2025· Prime Food Processing LLC.

Recalled Item: Lava Bun with Green Tea Flavor bright lime green packaging Recalled by Prime...

The Issue: Products do not declare milk in the Contains statement or the ingredient...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 14, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE...

The Issue: Ongoing investigations identified additional instances of the device...

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

Class II — Potential Health HazardOngoing