Reported Mar 15, 2017 · Terminated
ADVIA Centaur Progesterone; Catalog Number: 10310305 10315522 10333111 Product Usage: The PROG method is an in vitro…
Siemens Healthcare Diagnostics, 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: Siemens Healthcare Diagnostics, Inc · 333 Coney St · East Walpole, MA · 02032-1516
Is this the product you have?
- ADVIA Centaur Progesterone
- Catalog Number10310305 10315522 10333111
- Product UsageThe PROG method is an in vitro diagnostic test for the quantitative measurement of progesterone in human serum and plasma on the Dimension Vista¿System. Progesterone measurements are used in the diagnosis and treatment of disorders of the ovaries or placenta
- Lot codes and dates
- SMN10310305:
7542227483380274893892749947327487132751979627530565275386742754651527655704276669712767893427680930277
- SMN10315522:
743552748047627487497274202747772275148222752594327535303275432292764652527655505276674302768044827681415277
- SMN10333111: 84848274 89946274 14006275 33598275 49907276 66978276
- SMN10310305:
- Amount recalled
- 76,107
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
DHEA-S causes falsely elevated progesterone results.
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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