Boston Scientific recalls WATCHDOG Hemostasis Valve Kit (UPN H74939343A022/020) due to insertion tool occlusion preventing guidewire passage. Affected units include specific batch numbers and GTINs.
The firm received complaints of the Insertion Tool component being occluded, resulting in the inability to pass a guidewire through the tool.
Boston Scientific is recalling its WATCHDOG Hemostasis Valve Kit because the insertion tool may become occluded, preventing guidewire passage during medical procedures. This could lead to complications in procedures requiring vascular access.
The insertion tool in the kit can become blocked (occluded), making it impossible to pass a guidewire through the tool. This blockage could prevent proper vascular access during medical procedures, potentially causing complications.
Medical professionals using the WATCHDOG Hemostasis Valve Kit for vascular procedures are most at risk. Patients undergoing procedures with this kit may face complications if the insertion tool fails.
Check for the outer package UPN H74939343A022 and inner package UPN H74939343A020. Affected units include batch numbers 30272850, 30542947, 30661041, 30845826, and 30935565.
Verify the outer package UPN H74939343A022 and inner package UPN H74939343A020 with the listed batch numbers.
The firm received complaints of the Insertion Tool component being occluded, resulting in the inability to pass a guidewire through the tool.
Batch numbers 30272850, 30542947, 30661041, 30845826, and 30935565.
The recall record states the remedy is null, meaning no specific remedy is provided in this notice.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-1592-2023 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-1592-2023 from Boston Scientific. 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.
