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. 2,363 recalls have been distributed to North Dakota in the last 12 months.
Showing 24841–24860 of 27,512 recalls
Recalled Item: 00 4309-049-00 Trabecular Metal Reverse Shoulder Glenosphere Distractor Rx...
The Issue: Zimmer is initiating a lot specific recall of the Trabecular Metal" Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAVIS-EX Recalled by Nidek Inc Due to Under certain circumstances, the Left...
The Issue: Under certain circumstances, the Left eye image may be saved as the Right...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Soft Tissue Retractor Small Extendible. Offset blade facilitates...
The Issue: The small extendible Soft Tissue Retractor was recalled due to locking nut...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Tensioning Device The Synthes Osteogenesis System Recalled by...
The Issue: All lots of the Synthes Tensioning Device were recalled due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "***Flo Trac Sensor Model MHD85***" Sterile Recalled by Edwards...
The Issue: The Edwards Lifesciences FloTrac Sensor is being recalled due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Matrix Threaded Persuader Deformity is a comprehensive thoracolumbar...
The Issue: Synthes became aware that during a procedure using the Matrix Threaded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images...
The Issue: A limited number of endoscopes were shipped to FMSU-ESD with a manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slipped Capital Femoral Epiphysis System Product Usage: Intended for...
The Issue: There is a possibility for the Guide Wires of the Slipped Capital Femoral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recalled by Synthes...
The Issue: Specific lots of the SS 2.4mm and SS 2.7mm Locking Screw (self-tapping) due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used Recalled by...
The Issue: Complaints were received of inconsistencies in the expiration dates shown on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 46-Series Medical Washer-Disinfectors Recalled by Getinge...
The Issue: Getinge Disinfection AB initiated a voluntary field safety correction for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Part Numbers 79-43903 (3cc) Recalled by Stryker Craniomaxillofacial...
The Issue: Stryker received reports of the desiccant bag in the kit leaking silica gel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Anastaflo Intravascular Shunt Recalled by Edwards...
The Issue: Edwards Lifesciences is recalling certain lots of the Anastaflo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.