FDAApril 1, 2022device

11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VSE 11278VSEK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VSU 11278VSUK Flexible Video-Uretero-Renoscope (FLEX-XC) Z18447US-BC (03/2018); 11278VSUA 11278VSUAK Flexible Video-Ureter...

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

The hazard

Failure to achieve the expected six-log reduction in microorganisms following the disinfection process.

What to do

FDA enforcement status: Ongoing

Brands named

karl storz endoscopykarlkarl storz

UPCs

40485514025974048551416976404855134438540485514026034048551416969

Recall history

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

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11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VSE 11278VSEK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VSU 11278VSUK Flexible Video-Uretero-Renoscope (FLEX-XC) Z18447US-BC (03/2018); 11278VSUA 11278VSUAK Flexible Video-Ureter... — Recall Details · AllClear