Angiodynamics recalls DURAMAX Stacked Tip 24cm Basic Kit (Product # H787103028031) due to possible metal shavings causing surgical removal. Affected units sold with lot number 5809463.
Tri-Ball Tunneler may contain loosely affixed metal shavings, potential for the metal shaving to embolize, possibly requiring removal via surgical procedure.
Angiodynamics is recalling its DURAMAX Stacked Tip 24cm Basic Kit because it may contain metal shavings that could cause serious health issues requiring surgery. This recall affects users who have the specific product model with the listed lot number.
The product may contain loosely attached metal shavings that could become dislodged during use. If these shavings enter the bloodstream, they might cause blockages that require surgical removal to prevent serious health issues.
Users of the DURAMAX Stacked Tip 24cm Basic Kit (Product # H787103028031) with lot number 5809463 are affected. Those using the product for medical procedures are at higher risk due to potential internal complications.
Check for the product name 'DURAMAX Stacked Tip 24cm Basic Kit' with Product Number H787103028031 and Lot Number 5809463. The item was sold with a specific UDI-DI code 15051684011839.
Verify the product number H787103028031 and lot number 5809463 to confirm if your item is affected.
The recall states the product may contain metal shavings that could cause serious health issues requiring surgery, but the exact risk level isn't specified in the notice.
The recall notice does not provide specific action steps for affected users beyond checking product details.
Check for Product Number H787103028031 and Lot Number 5809463 on the item, as these are the identifiers for the recalled product.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1766-2024 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1766-2024 from Angiodynamics. 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.
