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RAPIDPOINT® 350 Sampler Module

Siemens Healthcare Diagnostics Inc. · Model 10375810 · UDI-DI 00630414566313

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1
510(k) clearances
105
Adverse events
5
Recalls
33
Facilities

Description

RAPIDPOINT® 350 Sampler Module, an in vitro diagnostics device to be used on the RAPIDPOINT® 350 analyzer

Recalls

DateFirmReason
2021-01-06Roche Diagnostics Operations, Inc.May display Calcium results on the screen with wrong arrow direction which may lead to misinterpretation of results and incorrect medical decision. If the unit for iCa++ is set to
2011-04-07Radiometer America IncBased on internal testing and user/customer complaint reports received, the firm determined that wrinkles may arise on the outer membrane of the calcium membrane units upon install
2008-09-05Radiometer America IncThe firm found that for this particular lot that the barcode, used for entering the characteristics of CAL1 Solution into the analyzer, does not reflect the actual values of the so
2005-09-29Radiometer America IncUnder certain circumstances, the ABL 700 & 800 Series Blood Gas Analyzers may experience leakage current into the measuring system. Consequently, the analyzers intermittently prov
2005-09-29Radiometer America IncUnder certain circumstances, the ABL 700 &800 Series Blood Gas Analyzers may experience leakage current into the measuring system. Consequently, the analyzers intermittently provid

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.