Angiodynamics recalls certain RS 5F DL BIOF: PASV kits due to potential unsafe levels of bacterial endotoxins. Affected kits have specific catalog and lot numbers. Consumers should contact the company for details.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics is recalling specific RS 5F DL BIOFLO PASV kits that may contain unsafe levels of bacterial endotoxins. This could pose a health risk if the kits are used improperly.
The kits may contain unsafe levels of bacterial endotoxins, which can cause fever or other health issues if the kits are used in medical procedures. This risk is related to the endotoxins in the kits.
Patients using the RS 5F DL BIOFLO PASV kits for medical procedures are most at risk. The recall affects specific catalog and lot numbers of these kits.
Check the catalog number 60M183481 and lot numbers 5301023, 5310193, or 5312020 on the kit packaging. The kits are sold by Angiodynamics.
Look for catalog number 60M183481 and lot numbers 5301023, 5310193, or 5312020 on the kit packaging.
The kits may contain unsafe levels of bacterial endotoxins, which can cause fever or other health issues.
Check the catalog number 60M183481 and lot numbers 5301023, 5310193, or 5312020 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-2214-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2214-2018 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.
