Reported Jul 1, 2015 · Terminated
VersaTREK Instrument Series 240 REF 6240, Manufactured for Remel Inc. The VersaTREK System is for cultivating and…
Remel 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: Remel Inc · 12076 Santa Fe Trail Dr · Lenexa, KS · 66215-3519
Is this the product you have?
- VersaTREK Instrument Series 240 REF 6240, Manufactured for Remel Inc. The VersaTREK System is for cultivating and recovering microorganisms, especially bacteria and yeasts, from blood and other normally sterile bodily fluids.
- Lot codes and dates
- Serial numbers
143 of 143 codes
016903920114062401690405011406260169050101141007016906860114121601690781011502132163X10132164X10132165X10132166X10132167X10132168X10132169X10132170X10132171X10132172X10132173X10132174X10132175X10132176X10132177X10132178X10132179X10132180X10132181X10132182X10132183X10132184X10132185X10132186X10132187X10132188X10132189X10132190X10132191X10132192X11132193X11132194X11132195X11132196X11132199X11132201X11132202X11132203X11132204X11132205X11132206X11132207X11132208X11132209X11132210X11132211X11132212X11132213X11132214X11132216X11132217X11132218X12132219X12132220X12132221X1213
- Serial numbers
- Amount recalled
- 143 devices
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Use of the recalled product may result in false positive reports.
This product could cause temporary or reversible health problems — stop using it.
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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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