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. 2,461 recalls have been distributed to North Dakota in the last 12 months.
Showing 16841–16860 of 27,512 recalls
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ¿ cobas c 6000 MODULAR Series System e Recalled by Roche...
The Issue: Roche has confirmed that a possible sample mismatch issue may occur on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic ENT Prgm 9734636 Add Fusion Nav AxiEM Recalled by Medtronic...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PPS RingLoc+ Acetabular Shell Recalled by Zimmer Biomet, Inc. Due to Device...
The Issue: Device was distributed with the etching missing from the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NON-STERILE SAMPLE Recalled by Sorin Group USA, Inc. Due to Medtronic...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMBLEM S-ICD Recalled by Boston Scientific Corporation Due to The device can...
The Issue: The device can deliver an atypical amount of energy due to memory corruption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMBLEM MRI S-ICD Model 219 Recalled by Boston Scientific Corporation Due to...
The Issue: The device can deliver an atypical amount of energy due to memory corruption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SQ-RX 1010 Pulse Generator Recalled by Boston Scientific Corporation Due to...
The Issue: The device can deliver an atypical amount of energy due to memory corruption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Straight Suction 9733449 EM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Curved Suction 70 9733450 EM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE SAMPLE SORIN GROUP Recalled by Sorin Group USA, Inc. Due to...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.