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. 2,556 recalls have been distributed to Hawaii in the last 12 months.
Showing 5461–5480 of 27,645 recalls
Recalled Item: Bronchoscope-for endoscopy and endoscopic surgery within the airways and...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Choleodochoscope. Model Numbers: CHF-BP30 Recalled by Aizu Olympus Co., Ltd....
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gastroscope-endoscopic ultrasound (EUS) guided fine needle aspiration (FNA)...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheal fiberscope-airway management Recalled by Aizu Olympus Co., Ltd. Due...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno fiberscope-For endoscopic diagnosis and treatment within the...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signmoidovideoscope-For endoscopy and endoscopic surgery within the lower...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hysterofiberscope-For endoscopic diagnosis within the uterus. Model Number:...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Small intestinal videoscope-For endoscopy and endoscopic surgery within the...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasonic gastrovideoscope-Real time ultrasound imaging Recalled by Aizu...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope: for endoscopy and endoscopic surgery within the lower digestive...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of...
The Issue: Units are labeled as 10cc; however the units have a fill volume of 1cc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus High-Flow Insufflation Unit Recalled by Olympus Corporation of the...
The Issue: There have been reports of patients suffering arrhythmias, reported as short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 Recalled by Philips North America Llc Due to Potential for...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex/Value Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8713051U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...
The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8713052U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...
The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi Navigation System Recalled by Acclarent, Inc. Due to When using...
The Issue: When using affected curette and software, there is a discrepancy between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Chest/Emergency Recalled by Philips North America Llc Due...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 Recalled by Philips North America Llc Due to Potential for...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.