Angiodynamics recalls RS 5F DL BIOFLO PICC kits with possible unsafe bacterial endotoxins. Affected units 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 certain PICC kits due to potential unsafe levels of bacterial endotoxins. This could cause fever or infection if used improperly. The recall affects specific model numbers and lot dates.
The kits might contain unsafe levels of bacterial endotoxins, which can cause fever or infection when used in medical procedures. This risk is related to the specific manufacturing process and quality control for these kits.
Patients using the RS 5F DL BIOF:PICC kits with catalog number 60M071831 and lot number 5310191 are most at risk. Healthcare providers who use these kits for medical procedures may also be affected.
Check for catalog number 60M071831 and lot number 5310191 on the kit packaging. The product was sold under the brand name Angiodynamics.
Reach out to Angiodynamics Inc. (Navilyst Medical Inc.) for specific instructions on how to handle the recalled kits.
The recalled kits have catalog number 60M071831 and lot number 5310191.
The recall states potential unsafe bacterial endotoxins, which could cause fever or infection, but not serious injury in normal use.
Look for catalog number 60M071831 and lot number 5310191 on the kit packaging.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2203-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2203-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
