FDAAugust 27, 2019device

Karl Storz, Model # 11161C2, Flexible Neuroscope

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

The hazard

During a complaint investigation it was determined that an error was observed within the instruction manual included with some scopes. Specifically, The Quick Connector Kits (QCK) and tray information, specified for the STERIS System 1E (SS1E) sterilization method within the instruction manual is incorrect. If the user uses SS1E to sterilize the impacted scopes and referred to the manual concerning the QCK information, the sterility of reprocessed scope cannot be guaranteed.

What to do

FDA enforcement status: Ongoing

Brands named

karl storz endoscopykarlkarl storz

Recall history

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

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