Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,146 recalls have been distributed to Ohio in the last 12 months.
Showing 8761–8780 of 55,415 recalls
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting instances of "Gas Loss in IAB Circuit" and "Gas Gain in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were experiencing a failure in the IAB Fiber Optic Sensor input on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were identifying autofill failure conditions on the devices causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting instances of "Gas Loss in IAB Circuit" and "Gas Gain in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users reported "System Over Temperature" alarms associated with a loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were experiencing a failure in the IAB Fiber Optic Sensor input on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were identifying autofill failure conditions on the devices causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting that the device was not charging as expected. It was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnifuse Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to The...
The Issue: The incorrect product labeling was applied to the product indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users reported "System Over Temperature" alarms associated with a loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: Users were reporting that the device was not charging as expected. It was...
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: 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: 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: EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V Recalled by Olympus...
The Issue: Recent reports of patient infection.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip Guide Catheter 8F 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 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 5F 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 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 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.