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U.S. Department of Health and Human Services

Class 2 Device Recall Vortex MPP5SDT Port

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 Class 2 Device Recall Vortex MPP5SDT Portsee related information
Date Initiated by FirmAugust 30, 2010
Date PostedAugust 24, 2011
Recall Status1 Terminated 3 on March 12, 2012
Recall NumberZ-3072-2011
Recall Event ID 59680
510(K)NumberK032754 
Product Classification Intravascular Catheter, Subcutaneous - Product Code LJT
ProductVortex MP Port Single Titanium Port with Attachable (5Fr) Silicone Catheter, AngioDynamics, Inc., One Horizon Way, Manchester, GA 30816 Indicated for central venous placement (either peripheral or chest placement) when patient therapy requires repeated venous access for injection or infusion therapy and/or venous blood sampling.
Code Information Catalog number: MP-P5SDT, Batch number: 513796 and 517058
Recalling Firm/
Manufacturer		 Angiodynamics, INC
1 Horizon Way
Manchester GA 31816-1749
For Additional Information ContactS. Michael Sharp, PhD
518-795-1123
Manufacturer Reason
for Recall		The labeling contains errors which result in the products being misbranded
FDA Determined
Cause 2		Labeling False and Misleading
ActionAngioDynamics, Inc. sent out a "Medical Device Recall" letter dated August 30, 2010 to all affected customers. The letter included; products affected, problem and asked them to return the product back to AngioDynamics. Customers were asked to fill out and return the included Recall Reply Form. For question on this recall contact AngioDynamics at (800) 772-6446.
Quantity in Commerce41 units
DistributionWorldwide Distribution: (USA) Nationwide distribution and the countries of Austria, China, Denmark, Egypt, France Germany, India, Italy, Latvia, Netherlands, Poland, Russian Federation, South Africa, Switzerland and the United Kingdom
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 = LJT
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