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  Class 2 Device Recall LINWOOD PORT ACCESS TRAY WITH HUBER NEEDLE see related information
Date Initiated by Firm March 31, 2011
Date Posted May 27, 2011
Recall Status1 Terminated 3 on September 13, 2011
Recall Number Z-2340-2011
Recall Event ID 58346
Product Classification Kit, i.V. Start - Product Code MCY
Product Material DT6110, PORT ACCESS TRAY WITH HUBER NEEDLE, LINWOOD, Distributed By: Midland Medical Supply Company 4850 Old Cheney Road Lincoln, Nebraska 68516 (402) 423-8877 (800) 742-2895, PORT ACCESS TRAY WITH HUBER NEEDLE, REORDER DT6110, STERILE..., LATEX FREE


Code Information BATCHES 2010062880, 2010080280, 2010091380, 2010102580 AND 2010120680. . . 
Recalling Firm/
Centurion Medical Products Corporation
100 Centurion Way
Williamston MI 48895-9086
For Additional Information Contact Lisa Carpenter
Manufacturer Reason
for Recall
This voluntary sub-recall was initiated because the vials of Bacteriostatic Sodium Chloride Injection, USP, 0.9% utilized to make the products may contain visible particulates.
FDA Determined
Cause 2
Material/Component Contamination
Action Centurion Medical Products Corporation issued press on April 1, 2011, and sent an Urgent Voluntary Recall letter dated March 15, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to discontinue use of the kits immediately and instructions were provided for the return of the kits. Customers were also asked to complete a form to fax or email back to the firm regarding the number of kits the firm has in their possession. Customers were instructed to provide recall notification to other firm's who received the recalled kits from their direct account. For any questions regarding this recall call 631-924-4000, ext 142.
Quantity in Commerce 345
Distribution Nationwide Distribution
Total Product Life Cycle TPLC Device Report

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.