Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to the sterile packaging (blister tray)...
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 America Inc directly.
Affected Products
Electrode, cutting, 24FR (27050G/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
Quantity: 9432 units
Why Was This Recalled?
Possible damage to the sterile packaging (blister tray) of some Karl Storz sterile products, which may result in airborne contamination.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Karl Storz Endoscopy America Inc
Karl Storz Endoscopy America Inc has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report