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Class 2 Device Recall YGlide (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass) |
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Date Initiated by Firm |
December 16, 2010 |
Date Posted |
February 14, 2011 |
Recall Status1 |
Terminated 3 on August 08, 2012 |
Recall Number |
Z-1225-2011 |
Recall Event ID |
57679 |
510(K)Number |
K072745 K934901 K003731
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Product Classification |
vascular interventional device - Product Code DTL
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Product |
Thomas Medical Products, Y-Glide (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass) for use during vascular interventional procedures. Part No. FTB-021-00, Catalog No. FTB-021-00. |
Code Information |
Part No. FTB-021-00, Catalog No. FTB-021-00, Lot #S32364 and Lot #S32528. |
Recalling Firm/ Manufacturer |
Thomas Medical Products Inc 65 Great Valley Pkwy Malvern PA 19355-1302
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For Additional Information Contact |
Tim Stoudt 610-651-5054
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Manufacturer Reason for Recall |
Compromised sterility/weak or open seals.
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FDA Determined Cause 2 |
Packaging process control |
Action |
GE Healthcare Thomas medical products Recall notification dated 16 December 2010 (GEHC Ref # 35003) was sent by letter via UPS Next Day Air and/or USPS certified mail. |
Quantity in Commerce |
28,679 for all products |
Distribution |
Distribution Nationwide USA and Germany. |
Total Product Life Cycle |
TPLC Device Report
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1 A record in this database is created when a firm initiates a correction or removal action. 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. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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510(K) Database |
510(K)s with Product Code = DTL and Original Applicant = THOMAS MEDICAL PRODUCTS, INC.
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