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. 2,557 recalls have been distributed to North Dakota in the last 12 months.
Showing 3441–3460 of 27,512 recalls
Recalled Item: Mazor X. Model Number Recalled by Mazor Robotics Ltd Due to Software...
The Issue: Software anomalies which can result in two separate issues: A lagging screen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PE Centrifuge Temperature Controlled Recalled by Beckman Coulter Biomedical...
The Issue: The adhesive joint between the plastic socket and metal component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Express Recalled by Beckman Coulter Biomedical GmbH Due to The...
The Issue: The adhesive joint between the plastic socket and metal component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PE Centrifuge Recalled by Beckman Coulter Biomedical GmbH Due to The...
The Issue: The adhesive joint between the plastic socket and metal component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter Healthcare...
The Issue: The Spectrum WBM may fail to auto-document infusion status information back...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter...
The Issue: The Spectrum WBM may fail to auto-document infusion status information back...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WAVEWRITER ALPHA: Model: SC-1216 Recalled by Boston Scientific...
The Issue: Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Firm has released a...
The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...
The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo...
The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TiBrid Stand Alone Intervertebral Body Fusion Device Recalled by Omnia...
The Issue: Failure of fusion system instruments in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TiBrid Stand Alone Intervertebral Body Fusion Device Recalled by Omnia...
The Issue: Failure of fusion system instruments in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: TOTAL PLUS Recalled by Alcon Research LLC Due to Alcon has...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SLIT FULL HANDLE2.6MM ANG DUAL Recalled...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SLIT FULL HANDLE2.75MM ANG DUA Recalled...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: A-OK 19G V-LANCE FULL HANDLE1.6MM SATIN Recalled...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT HP2 DB SLIT 3.0MM ANGCE Recalled by...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: ClearCut Sideport Knife Dual Bevel 1.2mm...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.