FDA Device Recalls

Recalls /

#43400

Product

Roche Elecsys total PSA, catalog number 11731262322.

FDA product code
LTJProstate-Specific Antigen (Psa) For Management Of Prostate Cancers
Device class
Class 2
Medical specialty
Immunology
PMA numbers
P990056S001
Affected lot / code info
Lot 171640.

Why it was recalled

There is the possibility of high results with sera expected to have non-detectable levels of tPSA if these reagent lots are used in combination on the Modular Analytics E170 analyzer.

Root cause (FDA determination)

Other

Action the firm took

Consignees were notified of the incompatibility via reagent bulletin dated 12/7/05.

Recalling firm

Firm
Roche Diagnostics Corp.
Address
9115 Hague Rd, Indianapolis, Indiana 46256-1025

Distribution

Distribution pattern
Nationwide.

Timeline

Recall initiated
2005-12-07
Posted by FDA
2006-01-11
Terminated
2006-02-26
Status

Source: openFDA Device Recall endpoint. Recall record ID #43400. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

— recall: Roche Elecsys total PSA, catalog number 11731262322. · FDA Device Recalls