Reported Jun 20, 2018 · Terminated
RS TANDEM 5F DL BIOFLO PASV, Catalog Number 60M232242
Angiodynamics Inc. (Navilyst Medical Inc.)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Angiodynamics Inc. (Navilyst Medical Inc.) · 10 Glens Falls Tech Park · Glens Falls, NY · 12801-3864
Is this the product you have?
RS TANDEM 5F DL BIOFLO PASVCatalog Number 60M232242
- Lot codes and dates
- UPNH96560M2322421
- Lot
53043245316020
- Amount recalled
- 20 boxes
This recall covers 38 products
The agency filed one notice per product. You are reading one of them; the other 37 are below.
25 more are in the archive.
Where it was sold
Why it was recalled
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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