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. 2,512 recalls have been distributed to Hawaii in the last 12 months.
Showing 12781–12800 of 27,645 recalls
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC-2000 Therapeutic Medical Laser System - Product Usage: Indicated for...
The Issue: Power supply (Model Number: TLC-2003) ME90A2403F01 (24 VDC, 3.75 A, 90 W, 1%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...
The Issue: Device was shipped without a Unique Device Identification (UDI) label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...
The Issue: Device was shipped without a Unique Device Identification (UDI) label and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ra Medical Systems DABRA Catheter 5F (1.5mm) Recalled by Ra Medical Systems,...
The Issue: The firm has become aware there is a potential problem with its DABRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/wing 5700LAX...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/knob...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical Philips M1355A Toco Transducer with belt wire/knob Recalled...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical Philips M1356A Ultrasound Transducer with belt/wire knob...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/wing (2264LAX)...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob Recalled by...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Recalled by Pacific...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MotoBand CP Recalled by CrossRoads Extremity Systems, LLC Due to Potentially...
The Issue: Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...
The Issue: An issue with the Detector for the Forte Family of cameras may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TherMax Blood Warmer Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: TherMax Blood Warmers may not be in compliance with an electrical safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrosurgical Tip Cleaner Product Usage: electrosurgical accessory...
The Issue: The sterile barrier of some devices may have been affected
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.