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. 2,415 recalls have been distributed to North Dakota in the last 12 months.
Showing 18561–18580 of 27,512 recalls
Recalled Item: SOMATOM Definition AS system Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Hardware issue that may expose the User to a potential risk for serious...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Reamer Handle Recalled by Greatbatch Medical Due to On June 14, 2016,...
The Issue: On June 14, 2016, Greatbatch discovered a significant increase in the number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 Assay (250 test kit)-for use Recalled by Siemens...
The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS Lyse Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the AQUIOS Lyse Reagent Kit because it may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReShape Integrated Dual Balloon System Recalled by Reshape Medical Inc Due...
The Issue: ReShape Medical is recalling the Integrated Dual Balloon System Gen 1 due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Precision Specimen Container- 4 oz (118 mL) Recalled by Covidien...
The Issue: Sterility of the outer surface of the container compromised due to packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD INLAY Ureteral Stent with Suture Recalled by C.R. Bard, Inc. Due to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Fluoro-4 Silicone Ureteral Stent Recalled by C.R. Bard, Inc. Due to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Totalis Recalled by C.R. Bard, Inc. Due to Labeling: Statement was added to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Inlay Optima¿ Multi-Length Ureteral Stent Coated Double Pigtail...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Algerbrush-II Product Usage: Medical - For surgeons to use in Recalled by...
The Issue: According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAMBRO Capillary Dialyzer Recalled by Baxter Healthcare Corp. Due to...
The Issue: Potential presence of particulate matter on the blood side of the dialyzer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage Total 5 Control Level 1 Recalled by Alere San Diego, Inc. Due...
The Issue: Encoded with incorrect ranges that are not consistent with the ranges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Lactic Acid Part # 09D891T21 The Lactic Acid assay Recalled by...
The Issue: Abbott has identified negative interference from the drug N-Acetyl Cysteine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiation Therapy Treatment Planning System Product Usage: RayStation is a...
The Issue: An error may occur with the display of dose computed on images other than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RF MultiGen¿ Recalled by Stryker Instruments Div. of Stryker Corporation Due...
The Issue: Stryker Instruments is voluntarily recalling the Care...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Algovita Spinal Cord Stimulation System Recalled by Nuvectra Due to Nuvectra...
The Issue: Nuvectra is conducting a recall due to two clinical risks that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Recalled by St Jude Medical Inc. Due to St Jude Medical is recalling...
The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fortify VR Recalled by St Jude Medical Inc. Due to St Jude Medical is...
The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to St Jude Medical is...
The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.