FDAJune 16, 2015device

Celsite Implantable Access Port System, model ST301. The Celsite Implantable Access Port Systems (Celsite port systems) are implantable port and catheter systems that allow safe, repeated access to the patient's bloodstream. The port chamber and catheter design can be used for the administration ...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The manufacturer, B. Braun medical France, received endotoxin test results that are out of specification for the peelable sheath (A1537).

What to do

FDA enforcement status: Terminated

Brands named

b braun interventional systems

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Celsite Implantable Access Port System, model ST301. The Celsite Implantable Access Port Systems (Celsite port systems) are implantable port and catheter systems that allow safe, repeated access to the patient's bloodstream. The port chamber and catheter design can be used for the administration ... — Recall Details · AllClear