Applied Medical Resources recalls STEALTH SPRING CLIP 6mm latis (1/4 Force) due to risk of inadequate vessel occlusion during cardiovascular procedures. Affected units manufactured July 5, 2019, with expiration July 3, 2024.
Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Applied Medical Resources recalls STEALTH SPRING CLIP 6mm latis (1/4 Force) because the device may fail to properly close blood vessels during surgery, potentially causing bleeding. This is a serious risk for patients undergoing cardiovascular or vascular procedures.
The clips may not seal blood vessels properly during surgery, leading to uncontrolled bleeding. This can cause serious complications like hemorrhage or death if the clip fails to maintain vessel occlusion.
Patients who received this clip during surgery are at risk. Healthcare providers using the device for cardiovascular procedures may need to stop using it immediately.
Check for the product name 'STEALTH SPRING CLIP 6mm latis (1/4 Force)' with lot number 1360356 manufactured on July 5, 2019, and expiring July 3, 2024.
Immediately stop using the STEALTH SPRING CLIP 6mm latis (1/4 Force) if it was used in surgery.
No, the product has been recalled due to a risk of inadequate vessel occlusion during surgery.
If you received this clip during surgery, stop using it immediately and contact your healthcare provider.
This product was manufactured on July 5, 2019, with an expiration date of July 3, 2024.
We’ve drafted a message you can send Applied Medical Resources Corp to request your refund or repair — edit it as you like.
Subject: Recall Z-2035-2020 — Applied Medical Resources Corp Applied Medical Resources Corp Hello, I own a Applied Medical Resources Corp that is covered by recall Z-2035-2020 from Applied Medical Resources Corp. 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.
