Genicon recalls single-use laparoscopic clip appliers (model 360-010-001) due to jamming and clip loading failures. Affected units sold with specific lot codes.
Device malfunction causing the applier to jam, and clip loading failures.
Genicon is recalling single-use laparoscopic clip appliers that can jam or fail to load clips. This could lead to improper surgical procedures if used during medical procedures.
The applier may jam during use, causing clips to fail to load properly. This could lead to improper surgical procedures if the clips are not applied correctly.
Surgical teams using the Genicon Li-Gator clip appliers for procedures involving tubular structures. Patients undergoing surgery with these devices are at risk of improper clip application.
Check for model number 360-010-001 with lot codes I8250 through I9719-A and J0113-A through J0243-A. These units were sold for use on tubular structures or vessels.
Identify the model number 360-010-001 with specific lot codes listed in the recall notice.
The recall is due to the applier potentially jamming and failing to load clips, which could lead to improper surgical procedures.
The recall notice does not specify a remedy, so check with Genicon for further instructions.
Yes, affected units have lot codes I8250 through I9719-A and J0113-A through J0243-A.
We’ve drafted a message you can send Genicon to request your refund or repair — edit it as you like.
Subject: Recall Z-0310-2021 — Genicon Genicon Hello, I own a Genicon that is covered by recall Z-0310-2021 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.