B. Braun Hyperformer EVA Mixing Container with Hyperformer Compatible Connector, 4000ml size, Catalog Number SH4000, Batch Numbers 05A14474, 05A18561, and 05A19926
This recall has been terminated (originally issued March 3, 2006).
- Company
- B. Braun Medical Inc
- Recall Initiated
- February 6, 2006
- Posted
- March 3, 2006
- Terminated
- May 28, 2008
- Recall Number
- Z-0586-06
- Quantity
- 13,480
- Firm Location
- Irvine, CA
- Official Source
- View on FDA website ↗
Reason for Recall
B. Braun Medical has been notified by the manufacturer of the product (Stedim) that a small percentage of the lots leak from the set port when the set port is opened. The leak was identified by Stedim to be due to the incorrect placement of a septum in the set port. The set closure is intact and the leak remains internal until the set port is opened.
Distribution
Nationwide to: CA, CT, FL, GA, KS, MD, MI, NC, NJ, NY, SC, TN, & TX
Lot / Code Info
Lot Numbers: 05A14474, 05A18561, & 05A19926
Root Cause
Other
Action Taken
A recall notification letter was sent to the 22 customers who received the product between 12/1/05 and 1/11/06. The recall packages included a letter addressed to either the Director of Pharmacy/Director of Nursing, Materials Manager, or Distributor, as appropriate. They were mailed via US Post Office certified return receipt mail. Customers were instructed by letter to return all product at their facility to B. Braun Medical, Inc. in Breinigsville Pennsylvania. A Recall Information Form and a postage paid B. Braun Medical, Inc. return envelope were included in the recall package for the customer''s use.