Angiodynamics recalls Bio-Stable 5F DL-... kits with possible bacterial endotoxins. Affected units may cause fever or infection. Contact for remedy.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics recalls certain Bio-Stable 5F medical kits due to potential bacterial endotoxins that could cause fever or infection. This is a safety issue for patients using these kits during procedures.
The kits might contain unsafe levels of bacterial endotoxins (pyrogens) which can cause fever or infection in patients during medical procedures. This is a potential health risk when the kits are used in clinical settings.
Patients undergoing medical procedures using the recalled kits are most at risk. Healthcare providers who use these kits for procedures may also be affected.
Check for the catalog number 45-895 on the kit packaging. The recall includes specific kits with UPN H965458950 and lot number 5304321.
Verify the catalog number 45-895 and lot number 5304321 on the kit packaging.
The recall states there might be unsafe levels of bacterial endotoxins, which could cause fever or infection. However, the risk level is low.
Check for catalog number 45-895, UPN H965458950, and lot number 5304321 on the kit packaging.
The recall does not specify a remedy, so contact Angiodynamics for further instructions.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2196-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2196-2018 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.
