Genicon recalls its GENILook Model 200-005-151 surgical cannula due to potential plastic tip detachment from the metal shaft. Affected units were sold with specific lot numbers and model identifiers.
There is potential for the plastic optical tip to become detached from the metal shaft.
Genicon is recalling its GENILook Model 200-005-151 cannula because the plastic optical tip might detach from the metal shaft. This could lead to the tip becoming a loose object during use, posing a risk of injury.
The plastic optical tip can become detached from the metal shaft during use. This could result in the tip becoming a loose object that might cause minor injury if it contacts the user or equipment.
Users of the Genicon GENILook Model 200-005-151 cannula, particularly those in medical settings, may be affected. The risk is low as the detachment is unlikely to cause serious injury.
Check for the Genicon GENILook Model 200-005-151 cannula with a 5mm diameter and 100mm length. Affected units were sold with specific lot numbers including I7920-F, I7951-F, I7957-F, I7985-F, I7850-F, I7902-F, and I8080-F.
Inspect the cannula for any signs of the plastic tip becoming loose or detached from the metal shaft.
The recall states there is potential for the plastic optical tip to become detached from the metal shaft, but the risk is low and does not typically cause serious injury.
The recall does not specify a remedy, so check for detachment and monitor the product for any signs of the tip becoming loose.
Affected units include lot numbers I7920-F, I7951-F, I7957-F, I7985-F, I7850-F, I7902-F, and I8080-F.
We’ve drafted a message you can send Genicon to request your refund or repair — edit it as you like.
Subject: Recall Z-2266-2020 — Genicon Genicon Hello, I own a Genicon that is covered by recall Z-2266-2020 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.
