Centeze Centesis Catheter, Catalog #: a) DRC-006-05, b) DRC-006-15,
FDA Recall Z-2563-2018 · Posted None
Recalling FirmGalt Medical Corporation
Recall StatusTerminated
Product CodeKGZ
Date Initiated2018-05-02
Date Terminated2020-07-20
Product Quantity300
Reason for Recall
The products listed might contain unsafe levels of bacterial endotoxins (Pyrogens) that were introduced during a manufacturing step. Bacterial Endotoxins also called pyrogenic bacteria can activate the inflammatory process and produce fever, chills, and hypotension in a patient.
Firm Action
On approximately 05/01/2018 recall letters and customer response forms were mailed to all consignees.
Root Cause
Other
Distribution Pattern
U.S.: MN, PA, VA, CA, UT, FL, NY, GA, LA, MO, TX, MS, OH, WA, MA, IL, KY, NC, and Puerto Rico; OUS: Canada, Australia, France, Germany, Ireland, Italy, Netherlands, Poland, Slovakia, Switzerland, Belgium, United Kingdom, Korea
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.