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U.S. Department of Health and Human Services

Class 2 Device Recall Crimper

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 Class 2 Device Recall Crimpersee related information
Date Initiated by FirmJanuary 20, 2014
Date PostedFebruary 03, 2014
Recall Status1 Terminated 3 on March 24, 2014
Recall NumberZ-0918-2014
Recall Event ID 67362
PMA NumberP100041 
Product Classification Aortic valve, prosthesis, percutaneously delivered - Product Code NPT
ProductCrimper Model 9100CR26 The Crimper is indicated for use in preparing the Edwards SAPIEN Transcatheter Heart Valve for implantation.
Code Information lot 59617777 and 59658495.
Recalling Firm/
Manufacturer		 Edwards Lifesciences, LLC
12050 Lone Peak Pkwy
Draper UT 84020-9414
For Additional Information ContactRobert Becker
801-565-5203
Manufacturer Reason
for Recall		Edwards Lifesciences is recalling two lot numbers of the 26mm transcatheter heart valve crimper because they may not open sufficiently when the handle is rotated in the full open position. As a result, user may have difficulty fitting a 26mm Sapien transcatheter heart valve into the crimper orifice when preparing the valve for crimping.
FDA Determined
Cause 2		Nonconforming Material/Component
ActionEdwards Lifesciences issued an Urgent Product Notice to all customers. Letters were sent via Fed Ex on 01/20/14. The letter outlines steps to be taken to enable a valve to fit into the open orifice, and allow the valve to be crimped according to normal instructions. Customers were instructed to forward the Urgent Product Notification letter to necessary personnel within their organization. Customers were also instructed to acknowledge they have reviewed and understand the notification letter by signing and dating the form included with the letter. Customers with questions were instructed to contact their Edwards Clinical Specialist.
Quantity in Commerce422
DistributionNationwide Distribution
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.
PMA DatabasePMAs with Product Code = NPT
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