FDA Device Intelligence
Home › SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD › IMMULITE®/IMMULITE® 1000 Systems DPD Pyrlinks-D

IMMULITE®/IMMULITE® 1000 Systems DPD Pyrlinks-D

SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Model 10381389 · UDI-DI 00630414964416

JMM
1
510(k) clearances
6
Adverse events
2
Recalls
10
Facilities

Description

Pyrilinks-D - IMMULITE - RGT - 100 Tests

Recalls

DateFirmReason
2013-04-25Roche Diagnostics Operations, Inc.Roche Diagnostics internal investigations in R&D have shown that the claims for biotin interference and the sample stability given in the Elecsys -CrossLaps (-CL) assay package ins
2012-08-10Immunodiagnostics Systems LtdIt has been noted by staff at IDS Inc. that stock of the affected products held at IDS Inc. are labeled with IVD labels although they are not registered for sale as IVDs in the Uni

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.