| Class 1 Device Recall Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Five Lumen Polyurethane | |
Date Initiated by Firm | October 04, 2010 |
Date Posted | February 23, 2011 |
Recall Status1 |
Terminated 3 on June 21, 2011 |
Recall Number | Z-1211-2011 |
Recall Event ID |
57663 |
510(K)Number | K081113 |
Product Classification |
Peripherally Inserted, Central Venous Catheter Tray - Product Code FOZ
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Product | Spectrum Central Venous Catheter Tray Minocycline/Rifampin Impregnated 5 Lumen Polyurethane, 10.0 Fr/ 20 cm, C-UQLMY-1001J-RSC-ABRM-HC-FST-A-RD, G51545, Sterile, Cook Medical, Cook Incorporated, Bloomington, IN. |
Code Information |
Part number: C-UQLMY-1001J-RSC-ABRM-HC-FST-A-RD, Global part number G51545. Lot numbers: 2272966, 2272967, 2298187. |
Recalling Firm/ Manufacturer |
Cook, Inc. 750 Daniels Way Bloomington IN 47404-9120
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For Additional Information Contact | Rita A. Harden 812-339-2235 |
Manufacturer Reason for Recall | Cook, Inc. is recalling Single, Double, Triple, and Five-Lumen Central Venous Catheter Trays AND Single and Double Lumen PICC Peripherally Inserted Central Venous Catheter Trays. These kits and trays contain 0.9% Sodium Chloride Injection USP 5 mL fill in 6 mL flush syringes that have been recalled by Excelsior Medical. During a routine test for syringe sterility, a possible integrity failure wa |
FDA Determined Cause 2 | Nonconforming Material/Component |
Action | Cook, Inc. sent URGENT DEVICE RECALLS letters to its customers dated 10/4/2010. The letters asked customers to examine their inventory and notify Cook for product return. The letter included a response form. |
Quantity in Commerce | 51, 473 trays all products |
Distribution | Worldwide distribution: USA, Chile, Colombia, Panama, Barbados, Canada, Guatemala, and Saudi Arabia. |
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 = FOZ
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