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. 2,535 recalls have been distributed to North Dakota in the last 12 months.
Showing 8641–8660 of 27,512 recalls
Recalled Item: Malosa Core LASIK Pack 2-Medical Kit- intended to be Recalled by Beaver...
The Issue: Kit packaging may have small holes compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Senior Living Arial Emergency and Nurse Call Systems Recalled by Stanley...
The Issue: Systems are not alarming due to increased memory consumption.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malosa Core Phaco Pack 1-Medical Cataract Kit intended to be Recalled by...
The Issue: Kit packaging may have small holes compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malosa Core Phaco Pack 2- Medical Kit intended to Recalled by Beaver Visitec...
The Issue: Kit packaging may have small holes compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malosa Core SMILE Pack 2-Beaver-Visitec- A Medical Kit intended Recalled by...
The Issue: Kit packaging may have small holes compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malosa Core Suface Treatment Pack -Medical Corneal Kit intended to Recalled...
The Issue: Kit packaging may have small holes compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas LiatSystem Recalled by Roche Molecular Systems, Inc. Due to Roche has...
The Issue: Roche has identified a small number of cobas Liat analyzer units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instavac Portable Suction Pump Recalled by Ohio Medical Corporation Due to...
The Issue: Increase in premature device failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultimum HEMOSTASIS INTRODUCER 5f 1.67 MM Recalled by Abbott Due to As a...
The Issue: As a result of a manufacturing error, one (1) lot of Ultimum Hemostasis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-75...
The Issue: Firm is initiating a correction due to the possibility of fluid ingress....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-31...
The Issue: Firm is initiating a correction due to the possibility of fluid ingress....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B...
The Issue: Due to a calculation error in the measurement when using 2D trace (manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray System with Azurion R2.2...
The Issue: (1)Start-up problem: Intermittently at start-up of the system, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Recalled by...
The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Recalled by...
The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair (with Recalled by...
The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BV Endura with Software Release 2.3- A mobile Recalled by Philips North...
The Issue: Instructions for Use do not specify the maximum surface temperature of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veradius Unity with Software Release 2.1- Amobile Recalled by Philips North...
The Issue: Instructions for Use do not specify the maximum surface temperature of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BV Pulsera with Software Release 2.3-A mobile Recalled by Philips North...
The Issue: Instructions for Use do not specify the maximum surface temperature of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stealthstation System w/ Stealthstation Cranial Software 3.1.1 Recalled by...
The Issue: Cranial biopsy procedure software can enter a state where the biopsy depth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.