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. 2,519 recalls have been distributed to Hawaii in the last 12 months.
Showing 11281–11300 of 47,764 recalls
Recalled Item: SX-One MicroKnife Recalled by SONEX HEALTH LLC Due to Potential of dull blade
The Issue: Potential of dull blade
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrogen Peroxide Topical Solution USP Recalled by Vi-Jon, LLC Due to Cross...
The Issue: Cross Contamination With Other Products: Product is cross contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HeartWare Ventricular Assist Device (HVAD) System Batteries Recalled by...
The Issue: Battery performance issues. Battery electrical faults render it unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use Recalled by...
The Issue: Falsely Elevated Atellica CH Microalbumin_2 (¿ALB_2) Results due to Reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Divalproex Sodium Delayed-Release Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: Failure occurred during routine stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Euphoria Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Euphoria Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Product Description/Item: ChemoLock Bag Spike Recalled by ICU Medical, Inc....
The Issue: Ports have a potential for unintended disconnection, inability to connect to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Description/Item: ChemoLock Vial Spike Recalled by ICU Medical, Inc....
The Issue: Ports have a potential for unintended disconnection, inability to connect to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-C6 Intensive Care Ventilator Recalled by Hamilton Medical AG Due to...
The Issue: Ventilator status indicator board can become loose, which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Stream Irrigation System (Catalog No. 5551000) and X-Stream Irrigation...
The Issue: The device may potentially cause a fire, leading to a safety risk.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Genesis II Non-Porous Tibial Baseplate Size 5 Right Recalled by Smith &...
The Issue: The product was mispackaged (swapped). The devices within the inner tray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrogen Peroxide Topical Solution Recalled by Vi-Jon, LLC Due to Labeling:...
The Issue: Labeling: Label Mix-Up-The primary label on the front of the bottles have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...
The Issue: Defective Delivery System: Customer complaints received for ripping patches...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Cholestech LDX¿ System combines enzymatic methodology and solidphase...
The Issue: Cholesterol test cassettes package insert is to be updated with new...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sprinter OTW Recalled by Medtronic Inc Due to Luer has balloon...
The Issue: Luer has balloon diameter printed as "2.25mmx12mm" instead of the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.