Applied Medical Resources recalls STEALTH SPRING CLIP 6mm latis (3/4 Force) due to potential failure to properly clamp blood vessels during surgery, risking bleeding. Affected units have specific lot numbers and dates.
Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Applied Medical Resources is recalling STEALTH SPRING CLIP 6mm latis (3/4 Force) devices because they may not properly close blood vessels during surgery, which could lead to bleeding. This recall affects medical devices used in cardiovascular and surgical procedures.
The clips may fail to seal blood vessels properly during surgery, potentially causing uncontrolled bleeding. This could lead to serious complications if the device is used in procedures where blood vessel occlusion is critical.
Medical professionals using the device during cardiovascular, peripheral vascular, or general surgery are most at risk. Patients receiving this device during procedures may also be affected.
Check for the product name 'STEALTH SPRING CLIP 6mm latis (3/4 Force)' with lot number 1357103 manufactured on June 4, 2019, and expiring June 2, 2024.
Verify the lot number and manufacture date on the device packaging.
The recall indicates a potential risk of inadequate vessel occlusion, so it is not recommended for use until the recall is addressed.
The recall does not specify a remedy, so contact the manufacturer for guidance.
The device was manufactured on June 4, 2019, with lot number 1357103.
We’ve drafted a message you can send Applied Medical Resources to request your refund or repair — edit it as you like.
Subject: Recall Z-2036-2020 — Applied Medical Resources Applied Medical Resources Hello, I own a Applied Medical Resources that is covered by recall Z-2036-2020 from Applied Medical Resources. 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.
