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. 2,375 recalls have been distributed to Hawaii in the last 12 months.
Showing 25881–25900 of 47,764 recalls
Recalled Item: Stanbio AC power adapter for the HemoPoint H2 meter Recalled by Stanbio...
The Issue: The US prong (type A) adapter plate may crack, break, or detach and remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT - Model no. 728326 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Flex - Model no. 728317 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Recalled...
The Issue: Device may display a battery missing error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GloCyte RBC Reagent - Product Usage: The GloCyte Automated Cell Recalled by...
The Issue: RBC Reagent failure. High fluorescent counts during RBC Reagent + Diluent QC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...
The Issue: Non-Sterility: Confirmed customer complaints of glass product container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...
The Issue: Non-Sterility: Confirmed customer complaints of glass product container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VOLISTA StandOP Surgical Light Recalled by GETINGE US SALES LLC Due to The...
The Issue: The manufacturer received complaints indicating that the device's central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear Recalled by ICU...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5" (13 cm) Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14 cm (5.5") Appx 0.27 ml Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Appx. 0.57 ml Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIT ORGANIC PEANUT BUTTER CHOCOLATE RASPBERRY bar NET WT 1.8 Recalled by...
The Issue: The firm was notified by the State of TN that the product contained...
Recommended Action: Do not consume. Return to store for a refund or discard.