Medrobotics recalls Obturator (shortcone) part 26114 due to potential rod separation. This component is used in Flex Rectoscope for robotic surgery. Affected units sold in specific lots.
The weld may break, resulting in the rod separating from the cone of the long and short cone Obturators.
Medrobotics is recalling a shortcone obturator part (number 26114) used in their Flex Rectoscope system. The recall is because the weld may break, causing the rod to separate from the cone, which could lead to surgical complications.
The weld in the obturator may break during use, causing the rod to separate from the cone. This separation could lead to surgical complications if the device fails during procedures.
Adults using Medrobotics Flex Robotic System for surgical procedures involving the anus, rectum, or distal colon. Patients and surgeons who have the specific lot numbers of the obturator part are most at risk.
Check if your obturator part has the model number 26114 and was sold in lots 19419-01, 19669-06, or 19684-06. This part is used in the Flex Rectoscope for robotic surgery.
Identify the lot number on your obturator part to see if it matches 19419-01, 19669-06, or 19684-06.
Reach out to Medrobotics for guidance on next steps if you have the recalled part.
The weld may break, causing the rod to separate from the cone, which could lead to surgical complications.
Yes, this obturator is a component of the Flex Rectoscope used in robotic surgery for adults (22 years and older).
Check if your obturator has model number 26114 and was sold in lots 19419-01, 19669-06, or 19684-06.
We’ve drafted a message you can send Medrobotics to request your refund or repair — edit it as you like.
Subject: Recall Z-1192-2019 — Medrobotics Medrobotics Hello, I own a Medrobotics that is covered by recall Z-1192-2019 from Medrobotics. 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.
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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.
