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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-0999-05
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 601276 ----WP1107 Wedge Press Cath.
Code Information Catalog Number: 601276. Lot Number, Exp. Date: 0060447424, 4/30/05; 0060449287, 4/30/05; 0060460591, 5/31/05; 0060461660, 6/30/05; 0060479198, 7/31/05; 0060485764, 8/31/05; 0060499554, 9/30/05; 0060503596, 10/31/05; 0060510910, 10/31/05; 0060534551, 12/31/05; 0060542987, 1/31/06; 0060551093, 2/28/06; 0060558251, 2/28/06; 0060563877, 3/31/06; 0060568298, 4/30/06; 0060577421, 4/30/06; 0060704964, 6/30/06; 0060707117, 8/31/06; 0060709910, 7/31/06; 0060720394, 9/30/06; 0060724488, 9/30/06; 0060724492, 10/31/06; 0060730638, 11/30/06; 0060733105, 11/30/06; 0060735054, 11/30/06; 0060741469, 12/31/06; 0060743202, 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 858 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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