Genicon recalls Model 210-005-151 cannulas due to risk of plastic tip detaching from metal shaft. Affected units sold in specific lots; check your product details to determine if recalled.
There is potential for the plastic optical tip to become detached from the metal shaft.
Genicon is recalling its Natura Model 210-005-151 cannulas because the plastic tip might detach from the metal shaft. This could cause the cannula to become unstable or malfunction during use.
The plastic optical tip can become detached from the metal shaft during use, potentially causing the cannula to become unstable or malfunction. This could lead to improper function or unintended movement of the device.
Users of the Genicon Natura Model 210-005-151 cannulas, particularly those using the product for medical or surgical purposes. The risk is low for most users as the detachment is unlikely to cause serious injury.
Check for the Genicon Natura Model 210-005-151 cannula with a 5mm diameter and 100mm length. Affected units were sold in specific lots labeled I8081-A, I7914-A, and I8033-A.
Identify your cannula model and lot number to determine if it is affected by this recall.
The recall indicates a potential for the plastic tip to detach from the metal shaft, but it is considered low risk as the detachment is unlikely to cause serious injury.
Check for the model number 210-005-151 with a 5mm diameter and 100mm length. Affected units were sold in specific lots labeled I8081-A, I7914-A, or I8033-A.
The recall does not specify a remedy, so you should check your product details to determine if it is affected. If it is, contact Genicon for further instructions.
We’ve drafted a message you can send Genicon to request your refund or repair — edit it as you like.
Subject: Recall Z-2274-2020 — Genicon Genicon Hello, I own a Genicon that is covered by recall Z-2274-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
