Genicon recalls its GENILook Model 200-005-251 surgical cannula due to potential plastic tip detachment from metal shaft. Affected units sold with lot number I9613-A.
There is potential for the plastic optical tip to become detached from the metal shaft.
Genicon is recalling its GENILook Model 200-005-251 surgical cannula because the plastic optical tip might detach from the metal shaft. This could cause the device to malfunction during use, potentially leading to injury if the detached tip causes unintended punctures.
The plastic optical tip can become detached from the metal shaft during use. If the tip separates, it might cause unintended punctures or injuries to the user or patient. This is a mechanical failure that could occur during surgical procedures.
Surgical professionals and medical facilities that purchased the Genicon GENILook Model 200-005-251 cannula with lot number I9613-A are likely affected. Those using the device for procedures where the cannula might be inserted into tissue are at higher risk.
Check for the Genicon GENILook Model 200-005-251 cannula with a 5mm diameter and 150mm length. The product was sold with lot number I9613-A. The universal handle can be used as a pistol grip or traditional Trocar handle.
Identify if your cannula has the model number 200-005-251 and lot number I9613-A.
The recall states there is potential for the plastic optical tip to become detached from the metal shaft, which could cause injury during use. However, the hazard is described as a low risk.
The recall does not specify a remedy, so you should check if your product matches the model and lot number described and contact Genicon for further guidance.
Look for the Genicon GENILook Model 200-005-251 cannula with a 5mm diameter, 150mm length, and lot number I9613-A.
We’ve drafted a message you can send Genicon to request your refund or repair — edit it as you like.
Subject: Recall Z-2269-2020 — Genicon Genicon Hello, I own a Genicon that is covered by recall Z-2269-2020 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.
