Angiodynamics recalls DURAMAX STACKED TIP 28 CM STRA: 5-UP PG for hemodialysis. Risk of serious injury if not used properly. Stop using and contact for remedy.
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Angiodynamics is recalling DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK catheters used for hemodialysis and apheresis. The recall is due to a risk of serious injury if the device is not used correctly.
The recall is due to a risk of serious injury if the device is not used correctly. However, the specific hazard mechanism is not clearly described in the recall notice.
Hemodialysis patients and healthcare providers who use the DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK catheters. Those most at risk are individuals with specific medical conditions requiring long-term vascular access.
Check for product number H787103028195 and UDI-DI 25051684011935. Lot numbers 5807195 and 5807196 are affected. The product is used for hemodialysis and apheresis.
Immediately stop using the DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK catheters if you have them.
DURAMAX STACKED TIP 28 CM STRAIGHT VASC-PAK catheters used for hemodialysis and apheresis.
The recall notice states a risk of serious injury if the device is not used correctly, but does not specify the exact hazard mechanism.
Check for product number H787103028195 and UDI-DI 25051684011935. Lot numbers 5807195 and 5807196 are affected.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1772-2024 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1772-2024 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.
