Learn more about medical device recalls.Ģ Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.ģ For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55. 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.
This Micro-Mate interchangeable syringe of a. Any questions contact: Phone: 40ġ A record in this database is created when a firm initiates a correction or removal action. These interchangeable syringes are manufactured to ensure the perfect mating of barrels and plungers.
#Micromate syringe series
This series of Microliter syringes is ideal for dispensing volumes from 0.25 L up to 5 L. 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. Characteristics: All are made from borosilicate glass metal parts are chrome-plated brass. The 600 series syringes are a half stroke version of the original 700 series syringes. Locate and quarantine all affected products.ģ. Accounts are requested to Recalled products must not be used.Ģ. 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. Micro-Mate Tuberculin Glass Syringe, Non-sterile Needle, aspiration and injection, disposable - Product Code GAA Class 2 Device Recall MicroMate Tuberculin Glass Syringe
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