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 8121–8140 of 27,512 recalls
Recalled Item: Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200...
The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare TDX SP2 Recalled by Invacare Corporation Due to The battery wiring...
The Issue: The battery wiring harness on affected wheelchairs may become disconnected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMARK Breast Biopsy Marker Recalled by Devicor Medical Products Inc Due...
The Issue: Small patient labels do not match the primary device label. The primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percept BrainSense Implantable Neurostimulator (INS) Recalled by Medtronic...
The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VerifyNow P2Y12 Test is designed to measure platelet P2Y12 Recalled by...
The Issue: Two whole blood Platelet Reactivity tests exist that share the same reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use Recalled by Medtronic Inc Due to Errors and...
The Issue: Errors and inconsistencies that were identified in the Instruction for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evans Wedge Disposable Trials Recalled by restor3d Inc. Due to During...
The Issue: During re-work of disposable instruments to relabel for 4-year shelf-life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Sterile Double Ended Trial Kit Recalled by restor3d Inc. Due to Product...
The Issue: Product labeled incorrectly. The lot was labeled with Small footprint when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evans Wedge Disposable Trials Recalled by restor3d Inc. Due to During...
The Issue: During re-work of disposable instruments to relabel for 4-year shelf-life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedMinder Medication Dispenser- Intended to serve as a medication reminder...
The Issue: Discontinuation of the Emergency Alert watch or pendant will no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Toe II Intramedullary Arthrodesis Implant Recalled by Stryker GmbH Due...
The Issue: The nickel-sensitivity statement on the outer carton may be partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific Recalled by...
The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific Recalled by...
The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products LH Reagent Pack Product Code: 1350198...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Prolactin Reagent Pack Product Code:...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products FSH Reagent Pack- IVD 1931922 Recalled by...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Uretero-reno videoscope Recalled by Olympus Corporation of the...
The Issue: The bending section of the URF-V2 may crack, resulting in an abnormal shape...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Recalled by Arthrex, Inc. Due to Products do not meet length and...
The Issue: Products do not meet length and diameter specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Medtronic formerly...
The Issue: The audible alarm may not sound and/or the omni-directional LED visual alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inactivated macrolide and quinolone-resistant Mycoplasma genitalium Recalled...
The Issue: QC process was not adequate for the specification range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.