Genicon recalls its GENILook Model 200-005-152 surgical device due to potential plastic tip detachment from metal shaft. Affected units sold with lot number I7717-C.
There is potential for the plastic optical tip to become detached from the metal shaft.
Genicon is recalling its GENILook Model 200-005-152 surgical device because the plastic optical tip might become detached from the metal shaft. This could cause the device to malfunction during use.
The plastic optical tip could become detached from the metal shaft during use, potentially causing the device to malfunction. This might lead to inaccurate targeting or unintended movement during surgical procedures.
Surgical professionals and medical facilities that own or use the Genicon GENILook Model 200-005-152 device with lot number I7717-C are affected. Those using the device for procedures where precise control is critical may be at slightly higher risk.
Check for the Genicon GENILook Model 200-005-152 device with a 5mm diameter and 100mm length. Affected units have lot number I7717-C and were sold with the universal handle design.
Verify if your device has the Genicon GENILook Model 200-005-152 with lot number I7717-C.
The recall states there is potential for the plastic optical tip to become detached from the metal shaft, which could cause malfunction during use. However, the hazard level is low risk.
Check for the Genicon GENILook Model 200-005-152 with 5mm diameter, 100mm length, and lot number I7717-C.
The recall does not specify a remedy, so you should check with Genicon directly for guidance.
We’ve drafted a message you can send Genicon to request your refund or repair — edit it as you like.
Subject: Recall Z-2267-2020 — Genicon Genicon Hello, I own a Genicon that is covered by recall Z-2267-2020 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.
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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.
