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. 2,391 recalls have been distributed to North Dakota in the last 12 months.
Showing 21381–21400 of 27,512 recalls
Recalled Item: Oxford Femoral Drill Guide Lateral IM Adapter Product Usage: Drill Recalled...
The Issue: Oxford Femoral Drill Guide Lateral IM Adapter may have an undersized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD Recalled by...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SERFAS 90 degree Energy Probe Recalled by Stryker Endoscopy Due to Stryker...
The Issue: Stryker Endoscopy is recalling all non expired SERFAS 90 degree Energy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVac 70 XTRA with Integrated Cable and PROcise EZ View Recalled by...
The Issue: Wands inspected with the adaptor fixture were released to the field not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurus 2500 Standalone Vitreous Probe Recalled by Alcon Research, Ltd. Due...
The Issue: Insufficient seal on the outside packaging, potentially affecting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SelectCore Variable Throw Biopsy Device Recalled by Stryker...
The Issue: Stryker Instruments is recalling the Stryker SelectCore Variable Throw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cannula and Seal Recalled by Stryker Sustainability Solutions Due to Stryker...
The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fios First Entry Recalled by Stryker Sustainability Solutions Due to Stryker...
The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...
The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...
The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laksell GammaPlan Recalled by Elekta, Inc. Due to Memory can become...
The Issue: Memory can become corrupted when creating a fused study via drag and drop in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...
The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Access System Recalled by Stryker Sustainability Solutions Due to...
The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...
The Issue: The double swivel connector may crack or separate on the endobronchial tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to Non-invasive...
The Issue: Non-invasive blood pressure pumps (NIBP) voltage is not sufficient and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.