Product Recalls in Connecticut

Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,485 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,485 in last 12 months

Showing 1758117600 of 28,245 recalls

Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Glenoid Reamer - Catalog #: 321-05-38 Recalled by...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2017· Merge Healthcare, Inc.

Recalled Item: Merge OrthoPACS software. The firm name on the label is Merge Healthcare...

The Issue: Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2017· Merge Healthcare, Inc.

Recalled Item: Merge OrthoPACS software. Recalled by Merge Healthcare, Inc. Due to A...

The Issue: A migrated study that has annotations will display the annotations, but when...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2017· NeuroLogica Corporation

Recalled Item: Samsung GU60A system- Digital X-ray Imaging Systems are intended for...

The Issue: When performing the Stitching function on GU60A system, unintended area is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Siemens Healthcare Diagnostics, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Shimadzu Medical Systems Usa Com

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Pentax of America Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Siemens Healthcare Diagnostics, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Pentax of America Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Siemens Healthcare Diagnostics, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Shimadzu Medical Systems Usa Com

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Siemens Healthcare Diagnostics, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Shimadzu Medical Systems Usa Com

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2017· Magellan Diagnostics, Inc.

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.

Class I — Serious Health HazardOngoing
Medical DeviceMay 23, 2017· Magellan Diagnostics, Inc.

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.

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Zimmer Periarticular Locking Plate System Recalled by Zimmer Biomet, Inc....

The Issue: Various trauma and extremity instruments (drill bits and screw taps) were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2017· Zimmer Biomet, Inc.

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.

Class II — Potential Health HazardOngoing