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U.S. Department of Health and Human Services

Class 2 Device Recall St. Jude Medical CPS Aim

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 Class 2 Device Recall St. Jude Medical CPS Aimsee related information
Date Initiated by FirmJune 01, 2006
Date PostedJune 24, 2006
Recall Status1 Terminated 3 on March 26, 2012
Recall NumberZ-1167-06
Recall Event ID 35616
510(K)NumberK053217 
Product Classification Catheter, Percutaneous - Product Code DQY
ProductCPS Aim, Models 410140, 410141, 410142, 410144, 410145, 410146, 410147, & 410148
Code Information All lots with a manufacturing date of May 30, 2006 or earlier
Recalling Firm/
Manufacturer		 St Jude Medical CRMD
15900 Valley View Ct
Sylmar CA 91342-3577
For Additional Information ContactNestor Kusnierz
818-493-2587
Manufacturer Reason
for Recall		Sterility-Some of the sterile pouches in which these products are packaged may not have been properly sealed during their packaging process.
FDA Determined
Cause 2		Other
ActionThe attached 'Dear Hospital Administrator' letter was sent out to our US sales representatives via FedEx on June 1, 2006. The sales representatives have been instructed to send back all of the devices in their inventory and to retrieve and return any remaining devices that were placed into hospital inventory. They are also instructed to deliver the attached 'Dear Hospital Administrator' letter to the appropriate person at each hospital where product is to be removed from the hospital shelf.
Quantity in Commerce4958
DistributionHospitals/Medical Centers in AZ, CA, MS, NY, & PA
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.
510(K) Database510(K)s with Product Code = DQY
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