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.
Showing 1041–1060 of 47,764 recalls
Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound System 1300 Recalled by B-K Medical A/S Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bk5000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UUltrasound System 2300 Recalled by B-K Medical A/S Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1202 Flex Focus Ultrasound System Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bk3000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bk3500 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Max Fusion XXX Recalled by Mohamed Hagar Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fasenra (benralizumab) Injection Recalled by ASTRAZENECA PHARMACEUTICALS Due...
The Issue: Lack of Assurance of Sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: or BS737162 Automated Digital Cell Morphology analyzer DI-60 Recalled by...
The Issue: Automated cell-locating device barcode reader may read the barcode of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Lithotriptor Recalled by Olympus Corporation of the Americas Due...
The Issue: The device may either fail to start up, or the transducer may start briefly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...
The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...
The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prazosin Hydrochloride Recalled by Teva Pharmaceuticals USA, Inc Due to CGMP...
The Issue: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbidopa Recalled by Rising Pharma Holding, Inc. Due to Product mix up:...
The Issue: Product mix up: complaint received that sealed medication bottle contained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SimplyGo Mini Recalled by Philips Respironics, Inc. Due to Certain serial...
The Issue: Certain serial numbers of the SimplyGo Mini standard battery kit contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM85 Digital Mobile X-ray imaging System Recalled by NeuroLogica Corporation...
The Issue: The four (4) M5 bolts that secure the Tube Head Unit to the end of the arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Good Neighbor Pharmacy Recalled by Trividia Health, Inc. Due to...
The Issue: Manufacturing defect causing LCD display issues with missing or partial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Desipramine Hydrochloride Tablets Recalled by Heritage Pharmaceuticals Inc...
The Issue: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Desipramine Hydrochloride Tablets Recalled by Heritage Pharmaceuticals Inc...
The Issue: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.