Angiodynamics recalls Bio-Stable 5F SL-... kits with possible bacterial endotoxins. Stop using if you have the kit with catalog number 45-886.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics is recalling Bio-Stable 5F SL-55CM IR-145 kits that may contain unsafe levels of bacterial endotoxins. This could cause fever or infection if used in medical procedures.
The kits might contain unsafe levels of bacterial endotoxins, which can cause fever or infection if introduced into the body during medical procedures.
Medical professionals who use these kits for procedures are most at risk. Patients using the kits under medical supervision are not directly affected.
Check for the catalog number 45-886 on the kit. The product was sold with UPN H965458860 and lot number 5303442.
Look for catalog number 45-886 on the kit label.
The recall states the kits might contain unsafe levels of bacterial endotoxins, which could cause fever or infection during medical procedures.
The recall does not specify a remedy, so check with your medical provider for guidance.
Look for catalog number 45-886 on the kit. The product was sold with UPN H965458860 and lot number 5303442.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2193-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2193-2018 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.
