Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Flexible Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to The action is being initiated due to intubation...
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
Flexible Intubation Fiberscope, Model # 11301AB1
Quantity: 14 scopes
Why Was This Recalled?
The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.
Where Was This Sold?
This product was distributed to 9 states: CA, CO, LA, ME, MO, NM, NY, OH, VA
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