Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,959 recalls have been distributed to Ohio in the last 12 months.
Showing 18761–18780 of 30,087 recalls
Recalled Item: SHIMADZU FDR Visionary Catalog Number: FDR Visionary Suite Stationary x-ray...
The Issue: Cracks may occur over time on the tube holding shaft near the base of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Protein 1 Control M Recalled by Siemens Healthcare...
The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIMADZU Ceiling Type X-ray Tube Support CH-200/CH-200M Catalog Number:...
The Issue: Cracks may occur over time on the tube holding shaft near the base of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Video Gastroscope Recalled by Pentax of America Inc Due to Error...
The Issue: Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Diagnostics LeadCare Ultra and LeadCare Plus test Kits. Product...
The Issue: Underestimates the lead concentration of venous blood samples when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Diagnostics LeadCare and LeadCare II test Kits. Product Usage:...
The Issue: Underestimates the lead concentration of venous blood samples when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Video Gastroscope Recalled by Pentax of America Inc Due to Error...
The Issue: Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Protein 1 Control H Recalled by Siemens Healthcare...
The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIMADZU RADspeed Pro Catalog Number: RADspeed Pro Recalled by Shimadzu...
The Issue: Cracks may occur over time on the tube holding shaft near the base of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Protein 1 Calibrator Recalled by Siemens Healthcare...
The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Protein 1 Control Recalled by Siemens Healthcare...
The Issue: Complaint of high amount of ceruloplasmin patient results below the range (<...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECT Internal Fixation Drill Bits 2.5 mm Diameter (0.98 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: The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended...
The Issue: Olympic Pasteurmatic 3000/3500 Systems are recalled because they do not...
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: PROMETRA II Programmable Infusion Pump Recalled by Flowonix Medical, Inc....
The Issue: Flowonix Medical received a report of a patient implanted with the Prometra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Periarticular Locking Plate System Drill Standard 2.7 mm Diameter...
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: Drill Bit Quick-Connect 3.2 mm Diameter 145 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: Drill Bit Quick-Connect 2.0 mm Diameter 100 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: ECT Internal Fracture Fixation Quick-Connect Drill 2.5 mm Diameter 12.5...
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 Femoral Drill 3.7 mm Diameter Replaces...
The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.