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. 2,363 recalls have been distributed to North Dakota in the last 12 months.
Showing 25841–25860 of 27,512 recalls
Recalled Item: Plum A+ Infusion Pump. List Number 11973. The Plum A+ Recalled by Hospira...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump. List Number 12391. The Plum A+ Recalled by Hospira...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Hyperbaric Infusion Pump. List Number 11005. The Plum Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump with Hospira MedNet Software. List Number Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of Malfunction S205 Backup Battery Failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of Malfunction S205 Backup Battery Failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...
The Issue: Observed instability of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineNet Anterior Cervical Cage Recalled by SpineNet Due to The recall...
The Issue: The recall decision has been made because because it has recently been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specialist 2 IM Rod Recalled by DePuy Orthopaedics, Inc. Due to Potential...
The Issue: Potential for the IM rod to break, leaving fragments in the patient....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoGastric Solutions EsophyX2 Plus Device with Serosa Fastener and...
The Issue: EsophyX2Plus device was not validated under actual or simulated use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to Incorrect...
The Issue: Incorrect packaging of regular set and fast set cartridges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gen-Probe LIFECODES PF4 Enhanced assay Recalled by Genetic Testing...
The Issue: Lifecodes PF4 Enhanced assay, lot number 3000389, is being recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to Incorrect...
The Issue: Incorrect packaging of regular set and fast set cartridges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to Symbiq Infusers...
The Issue: Symbiq Infusers have the potential to experience a white screen during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to Frequent Proximal...
The Issue: Frequent Proximal Occlusion Alarms (POAs) occurring on Symbiq devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to Symbiq Infusers...
The Issue: Symbiq Infusers have the potential to experience a white screen during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to Frequent Proximal...
The Issue: Frequent Proximal Occlusion Alarms (POAs) occurring on Symbiq devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...
The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Logic Comprehensive Knee Prosthesis System Recalled by Exactech,...
The Issue: A dimensional mismatch was identified which can potentially allow for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.