Karl Storz recalls flexible intubation fiberscopes with model #11301AB1 and specific lot numbers due to improper double port luer design. This may cause improper function during medical procedures.
The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.
Karl Storz is recalling flexible intubation fiberscopes with model number 113:01AB1 that were manufactured with a double port luer instead of a single port luer. This design flaw could lead to improper function during medical procedures.
The fiberscopes have a double port luer instead of a single port luer. This design flaw could cause improper function during medical procedures, potentially leading to incorrect intubation attempts.
Healthcare professionals using the recalled fiberscopes for intubation procedures are most at risk. Patients undergoing medical procedures with these devices may be affected.
Check for model number 11301AB1 on the device. The recalled lot numbers are 2183827, 2195794, 2215741, 2229258, 2235373, 2248169, and 2193769.
Verify the model number on the device is 11301AB1.
The recall is due to intubation scopes being improperly manufactured with a double port luer instead of a single port luer.
The official notice does not specify a remedy or action for affected users.
The affected lot numbers are 2183827, 2195794, 2215741, 2229258, 2235373, 2248169, and 2193769.
We’ve drafted a message you can send Karl Storz to request your refund or repair — edit it as you like.
Subject: Recall Z-2447-2019 — Karl Storz Karl Storz Hello, I own a Karl Storz that is covered by recall Z-2447-2019 from Karl Storz. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.