Loading...
Loading...
All product recalls associated with B. Braun Medical Inc.
Total Recalls
226
Past Year
32
Class I (Serious)
18
Most Recent
Oct 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
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.
package sealing defect - product may not be sterile
Tear away sheath assembly may contain a sheath (8FR) that is not the correct French size for the dilator (7FR).