![]() When one unit of blood has been collected (about 500 ml of blood plus volume of anticoagulant), it may be reinfused, or additional anticoagulant may be added to continue collection. Citrate phosphate dextrose adenine (CPDA-1) may also be used at a ratio of 1 ml per 7 ml of blood. The CPD injection may be facilitated by the use of a volume-control intravenous chamber run the desired amount of CPD into the chamber and then infuse the CPD via the intravenous tubing to the injection port.ī. When 1 unit of blood has been collected (about 500 ml total volume of blood plus CPD), it may be reinfused, or additional CPD may be added to continue the collection. Because it is difficult to estimate the amount of blood in a patient's chest, one approach is to instill enough CPD to anticoagulate one unit of blood initially (60 ml). One milliliter of CPD for every 7 ml of blood is recommended. Citrate phosphate dextrose (CPD) is a commonly used anticoagulant. Anticoagulant options include the following:Ī. If prescribed, inject anticoagulant into the collection unit as soon as possible during or before blood collection. Open all the clamps and make sure all the connections are airtight.ĩ. Remove the blue protective cap from the tubing on the A-1500 replacement bag and connect it to the Pleur-Evac tubing using the blue connectors.į. Remove the red protective cap from the collection tubing on the A-1500 replacement bag and connect it to the patient chest-drainage tubing using the red connectors.Į. Detach the red and the blue connectors.ĭ. Close the white clamp on the Pleur-Evac patient tubing and milk the blood distally from the tubing into the Pleur-Evac.Ĭ. Close the two white clamps on the top of the A-1500 replacement bag.ī. Use the foot hook and the ATS hanger on the side of the unit:Ī. Attach the autotransfusion bag (A-1500) to the side of the Pleur-Evac chest tube drainage system. Attach the autotransfusion bag if the unit is not ready for autotransfusion. Prophylactic broad-spectrum antibiotics may be given prior to reinfusion.Ĩ. Otherwise, blood that drains immediately on chest-tube insertion is lost to recovery.Ħ. This autotransfusion system requires prior assembly therefore consider routinely setting the autotransfusion component for patients who are at high risk for hemothorax. The physician or nurse practitioner inserts a large-bore chest tube(s).Ĥ. Assess for signs and symptoms of hypovolemia, hypoperfusion, and hemothorax.Ģ. 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 §7.55.1. ![]() 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. If you have no affected stock, please complete the Recall Acknowledgment Form and fax it to 1-85, Attn: Customer Service or email to you have any question please contact locals representative or Customer Service at 1-86.ġ A record in this database is created when a firm initiates a correction or removal action. To return product, complete the Recall Acknowledgement Form and fax it to 1-855- 419-8507, Attn: Customer Service or email to A customer service representative will contact you with a Return Goods Authorization (RGA) Number and will provide instructions for the return of products to Teleflex Medical.ģ. If you have affected stock in inventory, immediately discontinue use and quarantine any products with the product code and lot number listed, so that the affected products can be returned to Teleflex.Ģ. ![]() ![]() It states the following actions to be taken:ġ. Teleflex issued an "Urgent Medical Device Recall" notification on August 7, 2020. The thoracic catheter is indicated to be used in any surgical procedure requiring attachment to a Chest Drainage device. ![]()
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