Genicon recalls Model 200-105-152 optical tips due to potential plastic detachment from metal shaft. Affected units sold with lot I7781-C.
There is potential for the plastic optical tip to become detached from the metal shaft.
Genicon is recalling its GENILook Model 200-105-152 product because the plastic optical tip might detach from the metal shaft. This could cause the tip to become loose during use, potentially leading to injury if it breaks off.
The plastic optical tip can become detached from the metal shaft during normal use. If the tip breaks off, it could cause injury if it becomes a sharp object or if it gets stuck in the user's hand or equipment.
Users of the Genicon GENILook Model 200-105-152 with lot number I7781-C are affected. People using this product for medical procedures or other applications where precise handling is needed are most at risk.
Check for the Genicon GENILook Model 200-105-152 with a 5mm diameter and 100mm length (2 cannula). The lot number I7781-C is associated with this recall.
Inspect the plastic optical tip for signs of detachment from the metal shaft.
The recall states there is potential for the plastic optical tip to become detached from the metal shaft, which could cause injury if it breaks off.
Check for the Genicon GENILook Model 200-105-152 with a 5mm diameter, 100mm length (2 cannula), and lot number I7781-C.
The recall does not specify a remedy, so check for detachment and contact Genicon for further instructions.
We’ve drafted a message you can send Genicon to request your refund or repair — edit it as you like.
Subject: Recall Z-2271-2020 — Genicon Genicon Hello, I own a Genicon that is covered by recall Z-2271-2020 from Genicon. 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.