Angiodynamics recalls RS TANDEM 5F DL BIOFLO PICC kits with possible unsafe bacterial endotoxins. Affected units have specific catalog and lot numbers. Contact for remedy.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics recalls certain PICC line kits due to potential unsafe levels of bacterial endotoxins. This could cause fever or infection if used improperly. Affected kits have specific catalog and lot numbers.
Bacterial endotoxins in the kits can cause fever or infection if the kits are used improperly. This is a potential risk during medical procedures.
Patients using the RS TANDEM 5F DL BIOFLO PICC kits for medical procedures are most at risk. Healthcare providers who use these kits for patient care may also be affected.
Check for catalog number 60M250097 and lot numbers 5303198 or 5320749 on the kit packaging. The product was sold with UPN H96560M2500971.
Look for catalog number 60M250097 and lot numbers 5303198 or 5320749 on the kit packaging.
The kits might contain unsafe levels of bacterial endotoxins (pyrogens) which could cause fever or infection.
Check for catalog number 60M250097 and lot numbers 5303198 or 5320749 on the kit packaging.
The recall record 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-2216-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2216-2018 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.
