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. 2,503 recalls have been distributed to North Dakota in the last 12 months.
Showing 11361–11380 of 27,512 recalls
Recalled Item: Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re...
The Issue: The label on the cardbox and the blister show the correct symbols for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Radial Brown Recalled by Chengdu Ai Qin E-commerce Co., Ltd...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Black Starshine Recalled by Chengdu Ai Qin E-commerce Co.,...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Devil Red Recalled by Chengdu Ai Qin E-commerce Co., Ltd Due...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Diamonds Starlight Recalled by Chengdu Ai Qin E-commerce Co.,...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Flower Grey Recalled by Chengdu Ai Qin E-commerce Co., Ltd...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Flower Brown Recalled by Chengdu Ai Qin E-commerce Co., Ltd...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software versions syngo.CT VB20 or VB20_SP1 in the following systems:...
The Issue: Sporadic problems with the current software may result in scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARTO 3 System (Software Version V7.1.80) Recalled by Biosense Webster...
The Issue: Software defect may result in disapperance of tag sites during recalculation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE ONE Recalled by GE Healthcare, LLC Due to CARESCAPE ONE may not...
The Issue: CARESCAPE ONE may not provide visual and audible alarms for Ventricular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray System Recalled by Shanghai United Imaging...
The Issue: The metal edge overlap of the mylar strip in the gantry was uneven, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray System Recalled by Shanghai United Imaging...
The Issue: The metal edge overlap of the mylar strip in the gantry was uneven, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray System Recalled by Shanghai United Imaging...
The Issue: The metal edge overlap of the mylar strip in the gantry was uneven, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClosureFast Micro Introducer Sheath Set Recalled by Argon Medical Devices,...
The Issue: Sterile introducer sheath set manufactured under one lot with different...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci series System Control Module (SCM) Recalled by Abbott Gmbh & Co....
The Issue: Quality Control results were not properly evaluated for QC failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chembio DPP¿ Micro Reader for use with the DPP¿ COVID-19 Recalled by Chembio...
The Issue: FDA revocation of the Emergency Use Authorization due to performance issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chembio DPP COVID-19 IgM/IgG System- Rrapid immunochromatographic test for...
The Issue: FDA revocation of the Emergency Use Authorization due to performance issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chembio DPP¿ Micro Reader II for use with the DPP¿ Recalled by Chembio...
The Issue: FDA revocation of the Emergency Use Authorization due to performance issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anjon Bremer Molded Crown. bone fixation fastener for spinal use. Recalled...
The Issue: High rate of galling of one threaded component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Holder HKHZ 19 for use with Quadrox-i and Quadrox-iD Neonatal Recalled by...
The Issue: Removal for a specific lot, lot number 70128207, of Holder HKHZ 19 for use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.