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. 2,375 recalls have been distributed to North Dakota in the last 12 months.
Showing 24221–24240 of 27,512 recalls
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Intermittent noise on...
The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis Q and Artis Q biplane systems Product Usage: Recalled by...
The Issue: There exists the possibility that during clinical operation, a breakdown of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Update to...
The Issue: Update to correct the possibility for patients or operators to have their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8000 and 8015 with Alaris PCA Recalled by CareFusion...
The Issue: CareFusion is recalling the Alaris PC unit (model 8000 and 8015) because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CP5 centrifugal pump system Product Usage: The Stockert S5/ Sorin Recalled...
The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Recalled by...
The Issue: The recalling firm determined that visual inspections of the fork joints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic imaging systems (GEMINI LXL Model #882412 Recalled by Philips...
The Issue: The PET Reconstruction Server (PRS) database may randomly lock up after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5/C5 Heart-lung machine Product Usage: The StOckert S5/ Sorin C5 Recalled...
The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System (Brilliance CT Big Bore Oncology & Recalled...
The Issue: Machine Name in TumorLOC Basic Mode is obscured. When TumorLOC is in Basic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invivo Corporation Expression Information Portal (Model IP5) is intended to...
The Issue: Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach Irrigation Clip 40 Product Usage: Irrigation clips provide a...
The Issue: The Irrigation Clips were assembled with the incorrect (smaller) clips.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABACUS TPN Calculation Software Recalled by Baxter Corporation Englewood Due...
The Issue: Baxter Healthcare Corporation is issuing a voluntary correction for ABACUS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAS Omni Immune PRO Controls Recalled by Microgenics Corporation Due to The...
The Issue: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAS Omni Immune Controls Recalled by Microgenics Corporation Due to The...
The Issue: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: steroEOS Workstation with software versions: 1.3 Recalled by EOS Imaging Due...
The Issue: Error copying information to the clinical file and to the report when two 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carescape Patient Data Module The Patient Data Module Recalled...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular Screw 6.5mmx35mm Part Number: 010001000 Recalled by Biomet,...
The Issue: Investigation identified that the outer label, inner label, and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra LifeSciences is voluntarily recalling any unexpired lots of HITHSP10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Interlink threaded lock cannula This is a locking blunt Recalled by...
The Issue: BD Interlink Threaded Lock Cannula REF# 303369 and lot #3021392 is being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.