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U.S. Department of Health and Human Services

Class 2 Device Recall

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  Class 2 Device Recall see related information
Date Initiated by Firm May 25, 2005
Date Posted July 16, 2005
Recall Status1 Terminated 3 on December 14, 2006
Recall Number Z-1002-05
Recall Event ID 32177
510(K)Number K822806  K832287  K841639  
Product Classification Catheter, Flow Directed - Product Code DYG
Product Right Heart Catheter Product Line:
Catalog Number 604000------417D1006I.
Code Information Catalog Number 604000. Lot Number, Exp. Date: 0060444167, 3/31/05; 0060449163, 4/30/05; 0060451494, 4/30/05; 0060451497, 4/30/05; 0060460629, 6/30/05; 0060471018, 6/30/05; 0060480355, 7/31/05; 0060488611, 10/31/05; 0060537207, 1/31/06; 0060551137, 2/28/06; 0060554768, 2/28/06; 0060564022, 3/31/06; 0060575807, 4/30/06; 0060709793, 10/31/06; 0060721740, 9/30/06; 0060725206, 11/30/06; 0060725207, 11/30/06; 0060735650, 1/31/06; 0060743268, 1/31/06. 
Recalling Firm/
Manufacturer		 B. Braun Medical, Inc.
901 Marcon Blvd
Allentown PA 18109-9512
For Additional Information Contact Lori Sands
856-751-2080
Manufacturer Reason
for Recall		 Reports in a small percentage of Right Heart Catheter Products Line related to cracked catheter tips, leaking at the manifold and cracked hubs.
FDA Determined
Cause 2		 Other
Action The firm sent out recall notification letters to the Directors of Materials Management on 5/27/2005.
Quantity in Commerce 1281 units
Distribution Product was distributed to distributors and hospitals nationwide. Also, the products were distributed to Germany and Japan.
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.
510(K) Database 510(K)s with Product Code = DYG and Original Applicant = NOVA MEDICAL SPECIALTIES
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