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[Recalled] ADVIA Centaur¿ PSA Assay; Cat No. 06574155/SMN 10310292 (100 test)/02676506/SMN 10310293 (500 test) — Communication provided to emphasize that the PSA values should be interpreted i… | FDA 2016-08-09

recall fda device united-states

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

ProductADVIA Centaur¿ PSA Assay; Cat No. 06574155/SMN 10310292 (100 test)/02676506/SMN 10310293 (500 test)
Brand / manufacturerSiemens Healthcare Diagnostics, Inc
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2742-2016
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date09 August 2016
EAN / barcode10310292

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Communication provided to emphasize that the PSA values should be interpreted in accordance with current clinical guidelines for defining biochemical recurrence following radical prostatectomy.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Siemens Healthcare Diagnostics, Inc

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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