FDADecember 19, 2024device

KARL STORZ - ENDOSKOPE, REF: 27000L,Uretero-Renoscope, 7 Fr., 6¿, 43 cm, NON STERILE, RxONLY, CE 0123

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

The hazard

Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

What to do

FDA enforcement status: Ongoing

Brands named

karl storz endoscopykarlkarl storz

UPCs

04048551311271

Recall history

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

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