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. 2,448 recalls have been distributed to North Dakota in the last 12 months.
Showing 17321–17340 of 27,512 recalls
Recalled Item: Drill Bit Jacobs Chuck 3.2 mm Diameter 130 mm Length Recalled by Zimmer...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Calibrated Drill Long 4.3mm Recalled by Zimmer...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Drill 3.2 mm Diameter (.126 Inch) Recalled by...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Quick-Connect Drill 3.5 mm Diameter 11 cm...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Quick-Connect Drill 2.5 mm Diameter 11 cm...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Drill 2.5 mm Diameter (.098 Inch) Recalled by...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Drill 2.7 mm Diameter (.106 Inch) Recalled by...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Shank Drill Bit 4.0 mm Diameter Recalled by Zimmer Biomet, Inc. Due...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech 1.5" Novation Calcar Planer Guide Tip To assist the Recalled by...
The Issue: The firm determined that the labeling (surgical technique) should be updated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fracture Fixation Drill 4.5 mm Diameter (.177 Inch) Recalled by...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Distal Drill Pilot Tip 3.2 mm Diameter Recalled...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MULTIGENT Creatinine (Enzymatic) Recalled by Sentinel CH SPA Due to Reagent...
The Issue: Reagent 1 component may result in Quality Control values shifting out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Revolution EVO X-ray system Recalled by GE Healthcare, LLC Due...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30...
The Issue: An issue was discovered with the Pacific Hemostasis Fibrinogen Degradation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare lnnova IGS 540 ACT X-ray system Recalled by GE Healthcare, LLC...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare BrightSpeed X-ray system Recalled by GE Healthcare, LLC Due to...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery NM/CT 670 CZT X-ray system Recalled by GE...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery Ml X-ray system Recalled by GE Healthcare, LLC Due...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery PET/CT 600 Recalled by GE Healthcare, LLC Due to It...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lightspeed RT16 X-ray system Recalled by GE Healthcare, LLC...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.