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U.S. Department of Health and Human Services

Class 1 Device Recall Churchill Medical Systems

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 Class 1 Device Recall Churchill Medical Systemssee related information
Date Initiated by FirmApril 19, 2011
Date PostedJune 11, 2011
Recall Status1 Terminated 3 on June 18, 2012
Recall NumberZ-2390-2011
Recall Event ID 58794
Product Classification PICC insertion Tray - Product Code LKB
ProductChurchill Medical Systems AMS-8431CP (PICC insertion Tray). The device intended use is a PICC insertion tray.
Code Information Lot Number: 10H30.
Recalling Firm/
Manufacturer		 Vygon Corporation
103 A Park Drive
Montgomeryville PA 18936-9613
For Additional Information Contact
610-539-9300 Ext. 110
Manufacturer Reason
for Recall		Skin-Prep wipes purchased by Churchill (a Vygon company) for inclusion into Dressing Kits and PICC Insertion Kits were recalled by the manufacturer due to potential bacterial contamination.
FDA Determined
Cause 2		Nonconforming Material/Component
ActionA recall letter printed on Vygon letterhead dated April 20, 2011 and specific to each customer was sent via overnight courier mail. The letter described the affected product, issue and actions to take. Customers were instructed to check their inventory for the recalled products, cease use and distribution, and quarantine all affected product. Each customer received a custom copy of the letter with the specific product codes and lots that were shipped to them described in the Recall Acknowledgement and Inventory Return Form. Distributors were provided with instructions on how to handle product that was further distributed by them. The firm issued an updated Recall Notice dated May 31, 2011 to two consignees effected by the expanded recall. If you have any questions, please contact your local sales representative or Vygon's Customer Service Department at 1-800-473-5414, or by e-mail at customerservice@vygonus.com.
Quantity in Commerce1,500 units
DistributionUnited States (FL, MA, MD, and VA).
Total Product Life CycleTPLC 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.
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