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. 2,445 recalls have been distributed to Connecticut in the last 12 months.
Showing 29821–29840 of 51,038 recalls
Recalled Item: EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer Recalled by Exactech,...
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.
Recalled Item: EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Reamer // Catalog #:...
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.
Recalled Item: EXACTECH Equinoxe Modular Reverse Pilot-Tip Starter Reamer - Catalog #:...
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.
Recalled Item: LX3 Floor Stand for LuxOR Ophthalmic Microscope Recalled by Alcon Research,...
The Issue: Multiple shipments or forceful impact to a caster on a LuxOr/LX3 microscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Ultra-Fine(TM) needle ¿ mL 12.7mm 30G...
The Issue: Product mislabel. Lot 6291768 of the BD Insulin Syringes with the BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...
The Issue: Carestream found a single unit where four screws in the assembly were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
Recalled Item: Mefenamic Acid Recalled by Shionogi Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mefenamic Acid Capsules Recalled by Shionogi Inc. Due to Presence of foreign...
The Issue: Presence of foreign substance: The recall was initiated due to black...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PONSTEL (Mefanamic Acid) USP Recalled by Shionogi Inc. Due to Failed...
The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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 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: 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 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: 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.