B. Braun Medical, Inc. Right Heart Catheter Product Line: Catalog Number 601129-----5011094 0106 x 1007BBMWS. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Right Heart Catheter Product Line: Catalog Number 601129-----5011094 0106 x 1007BBMWS.
Brand
B. Braun Medical, Inc.
Lot Codes / Batch Numbers
Catalog Number: 601129. Lot Number, exp.date: 0060436563, 3/31/05, 0060449283, 4/30/05, 0060460576, 6/30/05, 0060478672, 7/31/05, 0060479191, 6/30/05, 0060485755, 7/31/05, 0060488734, 8/31/05, 0060496446, 9/30/05, 0060514308, 10/31/05, 0060520693, 11/30/05, 0060541501, 1/31/06, 0060551085, 2/28/06, 0060558243, 3/31/06, 0060572138, 4/30/06, 0060572440, 4/30/06, 0060577179, 5/31/06, 0060577413, 4/30/06, 0060706970, 6/30/06, 0060710249, 8/31/06, 0060721648, 9/30/06, 0060724465, 10/31/06, 0060732313, 10/31/06, 0060738463, 12/31/06, 0060746723, 1/31/06.
Products Sold
Catalog Number: 601129. Lot Number, exp.date: 0060436563, 3/31/05; 0060449283, 4/30/05; 0060460576, 6/30/05; 0060478672, 7/31/05; 0060479191, 6/30/05; 0060485755, 7/31/05; 0060488734, 8/31/05; 0060496446, 9/30/05; 0060514308, 10/31/05; 0060520693, 11/30/05; 0060541501, 1/31/06; 0060551085, 2/28/06; 0060558243, 3/31/06; 0060572138, 4/30/06; 0060572440, 4/30/06; 0060577179, 5/31/06; 0060577413, 4/30/06; 0060706970, 6/30/06; 0060710249, 8/31/06; 0060721648, 9/30/06; 0060724465, 10/31/06; 0060732313, 10/31/06; 0060738463, 12/31/06; 0060746723, 1/31/06.
B. Braun Medical, Inc. is recalling Right Heart Catheter Product Line: Catalog Number 601129-----5011094 0106 x 1007BBMWS. due to Reports in a small percentage of Right Heart Catheter Products Line related to cracked catheter tips, leaking at the manifold and cracked hubs.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Reports in a small percentage of Right Heart Catheter Products Line related to cracked catheter tips, leaking at the manifold and cracked hubs.
Recommended Action
Per FDA guidance
The firm sent out recall notification letters to the Directors of Materials Management on 5/27/2005.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026