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 26841–26860 of 47,764 recalls
Recalled Item: Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa Recalled by...
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument....
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14-442000S Antegrade Femoral Nail Instrument Kit Recalled by Zimmer Biomet,...
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Implantable Pulse Generator and Infinity 7 Implantable Pulse...
The Issue: Analysis of the difference between the actual device longevity and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim DRG Implantable Pulse Generator Model 3664 Recalled by St. Jude...
The Issue: Analysis of the difference between the actual device longevity and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Medical Kalare Fluoroscopic X-Ray System (DREX-KL80) Kalare is...
The Issue: During an examination images were displayed on the live monitor,but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Implantable Pulse Generator and Proclaim 7 Elite Recalled...
The Issue: Analysis of the difference between the actual device longevity and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeVest Wearable Defibrillator Model 4000 Recalled by Zoll Manufacturing...
The Issue: Incorrect service code for properly catching critical defects during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT DE handheld data processing module for clinical use Recalled by...
The Issue: Issues resulting from upgrade to software version 2.8: (1) Location,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex Fluorocell(R) PLT Fluorocell PLT is used to stain platelets Recalled...
The Issue: There is potential that fluorescent platelet (PLT-F) and immature platelet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fuji apples Recalled by Apple King, LLC Due to Fuji apples are recalled...
The Issue: Fuji apples are recalled because Thiabendazole was detected at 6.9 ppm.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Garden of Life Recalled by Garden Of Life, LLC Due to The product may pose a...
The Issue: The product may pose a choking hazard to newborns due to the thickness of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AutoCheck5+ Recalled by Radiometer America Inc Due to Radiometer has...
The Issue: Radiometer has recently become aware that a few of the AUTOCHECK 5+ level 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Organic Coconut Sugar Recalled by NOW Foods Due to Undeclared Gluten
The Issue: Undeclared gluten found in the product and the product is labeled "Gluten Free".
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Portex 1000 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intermed 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Prefilled 550 ml Sterile¿¿ ¿ Recalled by Medex Cardio-Pulmonary...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Prefilled 350 ml Sterile¿¿¿¿ ¿¿¿¿ ¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 500 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.