Applied Medical Resources recalls STEALTH SPRING CLIP 6mm latis (1/2 Force) due to failure to provide sufficient vessel occlusion during cardiovascular procedures. Affected units include specific lot numbers from June 2019 to June 2024.
Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Applied Medical Resources is recalling STEALTH SPRING CLIP 6mm latis (1/2 Force) devices because they may not properly close blood vessels during surgery, potentially leading to bleeding. This recall affects devices manufactured between June 2019 and June 2024 with specific lot numbers.
The cardiovascular clips may fail to seal blood vessels properly during surgery, which could result in uncontrolled bleeding. This risk occurs because the clips might not maintain adequate pressure on the vessel walls to prevent blood flow.
Surgical teams and medical professionals using the STEALTH SPRING CLIP 6mm latis during cardiovascular or vascular procedures are most at risk. The recall applies to specific lot numbers produced between June 2019 and June 2024.
Check for the lot number 1359929 on the device packaging or label. The product was manufactured on June 28, 2019, and expires on June 26, 2024.
Look for the lot number 1359929 on the device packaging or label to confirm if it is affected.
The recalled device is the STEALTH SPRING CLIP 6mm latis (1/2 Force).
The clips may fail to provide sufficient vessel occlusion during surgery, potentially causing uncontrolled bleeding.
The device was manufactured on June 28, 2019, with an expiration date of June 26, 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-2034-2020 — Applied Medical Resources Corp Applied Medical Resources Corp Hello, I own a Applied Medical Resources Corp that is covered by recall Z-2034-2020 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.
