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. 1,109 recalls have been distributed to Hawaii in the last 12 months.
Showing 1461–1480 of 47,764 recalls
Recalled Item: Getinge 88-Series Washer- Disinfector. Model Number: 88-5. Recalled by...
The Issue: Potential for device to overheat during operation if the circulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bevacizumab (Avastin) Injection Recalled by Fagron Compounding Services Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLEARLINK SYSTEM NON-DEHP CONTINU-FLO SOLN SET Recalled by Baxter Healthcare...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK SYSTEM EXTENSION SET Recalled by Baxter Healthcare Corporation Due...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK System Solution Set Recalled by Baxter Healthcare Corporation Due...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter. Model...
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter....
The Issue: Potential for breaches in the sterile barrier packaging, compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONTINU-FLO Solution Set Recalled by Baxter Healthcare Corporation Due to IV...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by Ascend Laboratories, LLC Due to Superpotent...
The Issue: Superpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...
The Issue: Failed Impurities/Degradation Specifications:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIOGRAPH One (DE). Model Number: 11689172. Recalled by Siemens Medical...
The Issue: There is a potential for an ice blockage to form or currently exist within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.