Genicon recalls Model 210-005-051 cannulas due to potential plastic tip detachment from metal shaft. This could cause injury during use. Affected units were sold with lot number I8003-A.
There is potential for the plastic optical tip to become detached from the metal shaft.
Genicon is recalling its Natura Model 210-005-051 cannulas because the plastic tip might detach from the metal shaft. This could lead to injury if the detached tip causes a puncture or cuts during use.
The plastic optical tip can become detached from the metal shaft during use. This detachment could cause the tip to move unexpectedly, potentially leading to minor injuries like cuts or punctures if it contacts sensitive areas.
Users of the Genicon Natura Model 210-005-051 cannulas, particularly those in medical or surgical settings, may be affected. The risk is low for most users as the product is designed for specific applications.
Check for the Genicon Natura Model 210-005-051 cannula with a 5mm diameter and 70mm length. The product was sold with lot number I8003-A for nonsterile samples.
Inspect the cannula for any signs of the plastic tip becoming loose or detached from the metal shaft.
The product is designed for specific use cases, but there is a potential risk of the plastic tip detaching from the metal shaft, which could cause minor injuries.
The recall does not specify a remedy, so check for detachment and consider contacting Genicon for further guidance.
Look for the Genicon Natura Model 210-005-051 cannula with a 5mm diameter, 70mm length, and lot number I8003-A for nonsterile samples.
We’ve drafted a message you can send Genicon to request your refund or repair — edit it as you like.
Subject: Recall Z-2273-2020 — Genicon Genicon Hello, I own a Genicon that is covered by recall Z-2273-2020 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.
