Product Recalls in New York
Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,178 recalls have been distributed to New York in the last 12 months.
Showing 5901–5920 of 30,153 recalls
Recalled Item: COOLIEF RF Generator is an 80-watt Radio-Frequency (RF) Generator with...
The Issue: Avanos has received an increase in complaints from customers for COOLIEF RF...
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 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: 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 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: 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 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 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 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 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 identifying autofill failure conditions on the devices causing...
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: 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 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 Airway Mobilescope 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 5F 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: 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 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.