The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Any questions contact: Phone: 40ġ A record in this database is created when a firm initiates a correction or removal action. If this information is received by a dealer, wholesaler, or distributor/reseller that distributed any of these products to other facilities, then notify their customers of this action so that those customers can locate and remove all affected products. Locate and quarantine all affected products.ģ. Accounts are requested to Recalled products must not be used.Ģ. The system integrates with industry-standard Cadence Virtuoso custom/analog, Cadence Innovus digital design, and mixed-signal flows.
#CADENCE SCIENCE MICROMATE VERIFICATION#
Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.Ĭadence issued the recall letter, specific to the customer dated 7/9/15 via registered mail on July 17, 2015. Cadence Physical Verification System (PVS) is the premier signoff solution enabling in-design and back-end physical verification, constraint validation, and reliability checking. Micro-Mate Tuberculin Glass Syringe, Non-sterile Needle, aspiration and injection, disposable - Product Code GAA Class 2 Device Recall MicroMate Tuberculin Glass Syringe