Windstone Medical recalls Angio Pack REF AMS8050A due to potential insufficient weld in angio tubing, which could cause leaks during medical procedures.
Angio tubing included within Custom Convenience kits may contain insufficient or incomplete weld
Windstone Medical is recalling Angio Pack REF AMS8050A because the angio tubing included in some kits may have insufficient or incomplete welds. This could lead to leaks during medical procedures, potentially causing complications for patients.
The angio tubing in the kit may have insufficient or incomplete welds, which could lead to leaks during medical procedures. This might cause complications such as fluid loss or contamination if the tubing fails under pressure.
Healthcare professionals using the Angio Pack REF AMS8050A kits for medical procedures are most at risk. Patients receiving procedures with these kits could be affected if leaks occur.
Check for the product name 'Angio Pack' with reference number AMS8050A. The kits were sold with specific lot numbers: 146305, 147637, 148389, and 148814.
Verify the product name and reference number on the packaging to confirm if it matches Angio Pack REF AMS8050A.
Reach out to Windstone Medical Packaging, Inc. for further assistance if you have the recalled product.
The angio tubing included in some kits may have insufficient or incomplete welds, which could lead to leaks during medical procedures.
Lot numbers 146305, 147637, 148389, and 148814 are affected.
Check the product details and contact Windstone Medical Packaging, Inc. for further assistance.
We’ve drafted a message you can send Windstone Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1849-2021 — Windstone Medical Windstone Medical Hello, I own a Windstone Medical that is covered by recall Z-1849-2021 from Windstone 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.
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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.
