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 5701–5720 of 27,645 recalls
Recalled Item: Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 5F 90CM MULTI PURPOSE Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 7F 100CM MULTI PURPOSE Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 8F PRE-SHAPED 40 90CM Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 8F 100CM MULTI PURPOSE Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 8F PRE-SHAPED 40 100CM Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 5F PRE-SHAPED 40 100CM Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 7F 90CM MULTI PURPOSE Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 6F 100CM MULTI PURPOSE Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 7F PRE-SHAPED 40 100CM Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 6F PRE-SHAPED 40 100CM Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 7F PRE-SHAPED 40 90CM Recalled by Boston...
The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henke-Ject-2 part luer sterile single use syringes - used for intravenous...
The Issue: Sterile barrier might be damaged compromising the sterility of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Distal Attachment (in Olympus Disposable EMR Kit)- Designed to...
The Issue: The Distal Attachment contain di-2-ethylhexyl phthalate (DEHP), which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable distal attachments Models: MH-462 Recalled by Aomori Olympus Co.,...
The Issue: The Distal Attachment contain di-2-ethylhexyl phthalate (DEHP), which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...
The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...
The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Tracheal Intubation Fiberscope Recalled by Olympus Corporation of...
The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...
The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...
The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.