Wilson-Cook Medical recalls Instinct Plus Endoscopic Clipping Device (REF G58010) due to potential malfunction. All units manufactured between September 2023 and April 2025 are affected. No remedy specified in recall notice.
Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.
Wilson-Cook Medical is recalling its Instinct Plus Endoscopic Clipping Device (REF G58010) because of potential malfunction. This device is used in medical procedures and could pose a risk if it fails during use.
The device may malfunction during medical procedures, potentially causing complications for patients. This could happen if the device fails to clip tissue properly or causes unintended tissue damage.
Medical professionals who use this device for endoscopic procedures are likely affected. Patients receiving this device during surgery may be at risk if it malfunctions.
Check for the product name 'Instinct Plus Endoscopic Clipping Device' and reference number G58010. The device was manufactured between September 2023 and April 2025.
Look for the reference number G58010 on the device packaging or label.
The recall states there is a potential for malfunction, but no specific safety issues have been confirmed.
Check for the reference number G58010 and verify the manufacturing date range from September 2023 to April 2025.
The recall does not specify any action steps; contact Wilson-Cook Medical for further guidance.
We’ve drafted a message you can send Wilson-Cook Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1812-2026 — Wilson-Cook Medical Wilson-Cook Medical Hello, I own a Wilson-Cook Medical that is covered by recall Z-1812-2026 from Wilson-Cook Medical. 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.
