Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs contain a reprocessing modalities that have...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Karl Storz Endoscopy directly.
Affected Products
KARL STORZ - ENDOSKOPE, REF: 27010K, Ureteroscope, 7 Fr., 34 cm, NON STERILE, RxONLY, CE 0123
Quantity: 3069 Units
Why Was This Recalled?
Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Karl Storz Endoscopy
Karl Storz Endoscopy has 70 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report