Cardiac tropnin (cTnl) assays were performed using the i-STAT I device.Įighty-nine cTnl levels were measured by both fingerstick and standard venipuncture. "When patients present complaining of chest pain, time can be critical to achieving positive outcomes, so Loyola was very keen to test this timesaving process." Currently Loyola is the only academic medical center in Chicago to utilize the i-STAT device.Ĭonducted in the Loyola Level 1 Trauma Center emergency department from June to August 2011, fingerstick blood samples were collected from consenting patients for whom standard-of-care venipuncture POC troponin (POCT) testing had been ordered as part of their workup. "Cardiac tropnin assays commonly exceed one hour while point-of-care testing can be completed in minutes by basic life support personnel," said Cichon, who is chair of the Emergency Medicine Department at Loyola. The study was conducted by Devin Loewenstein, BS, Christine Stake, MA and Mark Cichon, DO of Loyola University Chicago, Department of Emergency Medicine. 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 study was funded by the Department of Emergency Medicine, Loyola University Medical Center and was published in the American Journal of Emergency Medicine. 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. US: AK AL AZ CA CT DC FL GA HI IL IN KS KY MD MI MS NC NE NH NM NV NY OH OK OR PA SC SD TN TX VA WA WV WYġ A record in this database is created when a firm initiates a correction or removal action. We appreciate your understanding in this matter and thank you for your continued support of Abbott and Abbott products. If you have any questions regarding this information, please contact Abbott Point of Care Technical Support at 1-86, or via email at or contact your Abbott Point of Care support services representative. If you have forwarded any i-STAT cTnI blue cartridges to another facility, please provide a copy of this letter to them. If your facility repeatedly observes the i-STAT cTnI blue cartridges from a single lot generating a higher than expected number of QCCs, please contact APOC Technical Services for support and to report the information. Your Abbott Point of Care representative will contact you to discuss the details and timing of this transition for your facility. It further explains to customers while the i-STAT cTnI blue cartridges can continue to be used for patient testing, APOC recommends that all users of the i-STAT System be informed of the possibility of a higher than expected number of quality check codes while using the i-STAT cTnI blue cartridge and maintain a validated alternate backup method until the i-STAT cTnI white cartridges are received. The i-STAT cTnI blue cartridge, list number 06P23-25, will be discontinued for sale in the United States as of January 1, 2020. customers using the i-STAT cTnI blue cartridge, list number 06P23-25, to the i-STAT cTnI white cartridge, list number 03P90-25, beginning in November 2019. It explains Abbott Point of Care has made the decision to transition U.S. On Octothe firm distributed Urgent Medical Device Recall Communication letters by mail. The observed rate of quality check codes could be in the 3 to 5% range. I-STAT¿ cTnI blue cartridges may generate a higher than expected number of quality check codes. Immunoassay method, troponin subunit - Product Code MMI Class 2 Device Recall iSTAT cTnI cartridge
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