Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,540 recalls have been distributed to North Dakota in the last 12 months.
Showing 6741–6760 of 27,512 recalls
Recalled Item: Medtronic Grafton Plus Paste a) DBM S45001 GRAFTON 1CC PASTE Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Matrix Strips: a) DBM S42275 8MMX1CMX10CM 2EA MATRIX STRPS...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Putty: a) DBM S43101 GRAFTON 0.5CC PUTTY Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton DBF: a) PUTTY T50101 GRAFTON DBF 1CC Recalled by Medtronic...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Accelerate Grafton DBF a) ACCELERATE BG SET T50203 GRAFTON DBF 3CC...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Grafton Flex: a) DBM S42090 GRAFTON 1.5CM X 1.5CM FLEX Recalled by...
The Issue: Potential for packaging non-conformances directly related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System PA Sensor and Delivery System Recalled by St. Jude...
The Issue: Select CardioMEMS PA Sensors (Model CM2000) operate outside of the intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: There have been reported failures of the high pressure helium regulator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System PA Sensor and Delivery System Recalled by St. Jude...
The Issue: Select CardioMEMS PA Sensors (Model CM2000) operate outside of the intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump. Model Numbers: D998-00-0800-31...
The Issue: Firm has received reports of damaged, worn, or torn O-rings on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue. Model Number: 0998-00-0800-83. Recalled by Datascope...
The Issue: Firm has received reports of damaged, worn, or torn O-rings on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Model Nos. 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33...
The Issue: An unexpected shutdown of the IABP may occur due to loss of communication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System PA Sensor and Delivery System Recalled by St. Jude...
The Issue: Select CardioMEMS PA Sensors (Model CM2000) operate outside of the intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System Hospital Electronics System (HES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System Patient Electronics System (PES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System Patient Electronics System (PES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: There have been reported failures of the high pressure helium regulator,...
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: An unexpected shutdown of the IABP may occur due to a failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Model Nos. 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85...
The Issue: An unexpected shutdown of the IABP may occur due to loss of communication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS HF System Patient Electronics System (PES) Recalled by St. Jude...
The Issue: Radiated Radiofrequency (RF) emissions of the CardioMEMS Patient Electronics...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.