U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
데이터 추가 비고
Agent, absorbable hemostatic, collagen based - Product Code LMF
원인
The lyophilized thrombin component of the surgiflo hemostatic matrix kit with thrombin has the potential to be non-sterile due to an undetected air leak which occurred during the manufacturing process.
조치
Ethicon Inc. sent a Urgent Voluntary Product Recall letter dated April 3, 2012, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer.
If you have any product subject to this voluntary recall, please remove it from your inventory immediately and return it per the following instructions.
Return product to Stericycle using the enclosed pre-paid shipping label.
Shipping fees wil be charged directly to Ethicon through the use of this shipping label. No reimbursements will be made for the shipping charge if this label is not used. Extra shipping labels may be obtained by calling 1-866-338-2611. Credit will be issued for impacted product that is returned.
Further questions please call 1-866-338-2611, or contact your Ethicon Biosurgery Sales Representative.
Thank you for your coorporation and immediate assistance.
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Ethicon Surgiflo Hemostatic Matrix Kit with Thrombin Plus Flex Tip || Distributed by Ethicon Ethicon Inc., Somerville, NJ 08876 USA || Manufactured by Ferrosan Medical Devices || Ferrosan Medical Devices A/S || Sydmarken 5, DK-2860 Soeberg, Denmark || Mixed with sterile saline or thrombin solution is indicated for surgical procedures (except opthalmic) for hemostasis when control of capillary, venous and arteriolar bleeding by pressure, ligature, and other conventional procedures is ineffective or impractical.