Boston Scientific recalls 20-pack Watchdog Accessory Kit (UPN H74939343A021/020) 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 a 20-pack Watchdog Accessory Kit because the Insertion Tool can become occluded, making it impossible to pass a guidewire. This could prevent successful medical procedures if the kit is used without replacement.
The Insertion Tool component can become occluded during use, which blocks the guidewire from passing through the tool. This may prevent successful catheter procedures if the kit is used without replacement.
Medical professionals using the Watchdog Accessory Kit for catheter procedures are most at risk. The recall affects specific batch numbers and GTINs sold through medical suppliers.
Check for outer package UPN H74939343A021 or inner package UPN H74939343A020. The kit includes specific batch numbers and GTINs listed in the recall notice.
Look for outer package UPN H74939343A021 or inner package UPN H74939343A020 on the product.
The recall is for a potential issue with the Insertion Tool occlusion, but it does not pose a risk of serious injury. The hazard is described as a possible blockage during use.
Check for outer package UPN H74939343A021 or inner package UPN H74939343A020, and verify the batch numbers listed in the recall notice.
The recall does not specify a remedy, so no action is required. However, you should check the package details to confirm if your kit is affected.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-1593-2023 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-1593-2023 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.
