Genicon recalls Model 210-005-152 surgical cannulas due to potential plastic tip detachment from metal shaft. Affected units sold in specific lots; contact for remedy.
There is potential for the plastic optical tip to become detached from the metal shaft.
Genicon is recalling its Natura Model 210-005-152 cannulas because the plastic tip might detach from the metal shaft. This could cause injury during use, so affected owners should stop using the product immediately.
The plastic optical tip can become detached from the metal shaft during use, which may lead to the tip becoming a sharp object that could cause injury. This is especially concerning in medical procedures where precise control is needed.
Users of the Genicon Natura Model 210-005-152 cannulas, particularly those in medical settings where precise handling is critical. Medical professionals using these cannulas for procedures are at higher risk.
Check for the Genicon Natura Model 210-005-152 cannulas with 5mm diameter and 100mm length. The product was sold in specific lots labeled I7968-A and I8182-A.
Immediately stop using the Genicon Natura Model 210-005-152 cannulas if you have them, as the plastic tip may detach during use.
The plastic optical tip may detach from the metal shaft, which could cause injury during use.
Stop using it immediately and contact Genicon for further instructions.
Lots I7968-A and I8182-A.
We’ve drafted a message you can send Genicon to request your refund or repair — edit it as you like.
Subject: Recall Z-2275-2020 — Genicon Genicon Hello, I own a Genicon that is covered by recall Z-2275-2020 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.
