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Manufacturers
Roche Diagnostics GmbH
Manufacturer Parent Company (2017)
Roche Holding AG
Source
AEMPSVFOI
45 Events
Recall Or Safety Alert for • Accu-Chek® Spirit insulin pump, reference 05126347001 and • Accu-Chek® Spirit Combo insulin pump, reference 05458480001, manufactured by Roche Diagnostics GmbH, Germany
Recall Or Safety Alert for Multiplate® Analyzer
Recall Or Safety Alert for Cobas HIV-1 tests, ref. 06979599190 and Cobas HBV, ref. 06979564190, for use in the Cobas 4800 System.
Recall Or Safety Alert for Elecsys Anti-HAV test, reference 04854977190
Recall Or Safety Alert for Systems cobas p 612 pre-analytical system.
Recall Or Safety Alert for Cobas systems b 123 POC software version 4.7 (SW V4.7), references 05122287001 and 05064694001.
Recall Or Safety Alert for GLU / LAC / UREA cassettes (BUN) in the Cobas system b 221 <6˃
Recall Or Safety Alert for Tina-quant Hemoglonine A1c Gen.2 test, reference 04528123-190, used in the COBAS INTEGRA® 400 plus and 800 systems, and cobas c 311/501/502
Recall Or Safety Alert for sample rack trays
Recall Or Safety Alert for urine test strips Combur-Test®
Recall Or Safety Alert for ONLINE reagents TDM for Gentamicin
Recall Or Safety Alert for ONLINE reagents TDM for Gentamicin
Recall Or Safety Alert for Multiplate® Analyzer, reference 06675069001.
Recall Or Safety Alert for Reagents for Gentamicin
Recall Or Safety Alert for Reagents for Vancomycin: ONLINE TDM Vancomycon 100 tets, reference 04491050190, ONLINE TDM Vancomycon 200 tets, reference 05108420190, HITACHI VANCOMYCIN (911, 912, 917, P), reference 04642490190
Recall Or Safety Alert for cobas® EGFR Mutation test and the cobas® cfDNA sample preparation kit
Recall Or Safety Alert for Tests of Estradiol II, reference 03000079190 and Estradiol III, reference 06656021190
Recall Or Safety Alert for cobas p 512 systems
Recall Or Safety Alert for Handheld Platform Meters (Accu-Chek Inform II, CoaguChek Professional and cobas h 232)
Recall Or Safety Alert for Cobas b 123 Sensor Cartridges BG / ISE / GLU / LAC of the POC cobas b 123 systems, reference 05170478001.
Recall Or Safety Alert for Cobas 6800 systems
Recall Or Safety Alert for Test for the determination of uric acid in blood "Reflotron", reference 10745103203
Recall Or Safety Alert for Test for the determination of uric acid in blood "Reflotron", reference 10745103203
Recall Or Safety Alert for Fluid packs cobas b 123
Recall Or Safety Alert for Fluid packs cobas b 123
Recall Or Safety Alert for POC cobas b123 system, reference 05122287001
Recall Or Safety Alert for Test Tina-quant D-Dimer Gen.2 (100 tests), Ref .: 04912551190
Recall Or Safety Alert for CREA plus, CREP2, LACT2, Lactate, GLU, TRIGL / TG, CHOL / CHOL2, HDL-C plus 3rd generation / HDLC3, LDL_C plus 2nd generation / LDL_C, UA2 / UA plus
Recall Or Safety Alert for Elecsys CMV IgM test, reference 04784618-190, used in combination with some specific batches of Diluent Universal reference 03183971-122
Recall Or Safety Alert for Enzymatic Assay of homocysteine HCYS: Reference 05 385 415 190 HCYS, lot 69781101 and Reference 06 542 921 190 HCYS, lot 69781401
Recall Or Safety Alert for Kit Cobas® KRAS Mutation
Recall Or Safety Alert for Systems Cobas b 221 <6˃ / OMNI S6
Recall Or Safety Alert for Systems "Cobas b 221"
Recall Or Safety Alert for Analyzers "Cobas b 121" and "Cobas b 221"
Recall Or Safety Alert for Accu-Chek® Spirit Combo insulin pump, model 00700006863
Recall Or Safety Alert for Systems Cobas b 221 <6> / OMNI S6
Recall Or Safety Alert for Calcium Gen.2 (CA2)
Recall Or Safety Alert for Accu-Chek® Compact test strips and Accu-chek Compact Plus blood glucose meters
Recall Or Safety Alert for Cobas 8000 analyzers that use the cobas c 502 module and reagent cassette cobas c pack MULTI
Recall Or Safety Alert for Elecsys HIV combi PT assay
Recall Or Safety Alert for rack packs (reagent kit) of certain batch numbers of the Elecsys HIV combi PT assay
Recall Or Safety Alert for Systems "COBAS INTEGRA 800", catalog number 28122474001, with software version 9864.C2 installed
Recall Or Safety Alert for Certain CoaguChek® XS, CoaguChek® XS Pro and CoaguChek® XS Plus systems
Recall Or Safety Alert for Reactive strips Reflotron-Hemoglobin 30 Str.
Recall Or Safety Alert for Cobas Integra 400 and 400 plus systems and instruments, and Cobas 8000 Data Manager
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42 devices in the database
• Accu-Chek® Spirit insulin pump, reference 05126347001 and • Accu-Chek® Spirit Combo insulin pum...
Model / Serial
Multiplate® Analyzer
Model / Serial
Cobas HIV-1 tests, ref. 06979599190 and Cobas HBV, ref. 06979564190, for use in the Cobas 4800 Sy...
Model / Serial
Elecsys Anti-HAV test, reference 04854977190
Model / Serial
Systems cobas p 612 pre-analytical system.
Model / Serial
37 more
60 manufacturers with a similar name
Learn more about the data
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ROCHE DIAGNOSTICS GMBH
Manufacturer Parent Company (2017)
Roche Holding AG
Source
NIDFSINVIMA
Roche Diagnostics GMBH
Manufacturer Parent Company (2017)
Roche Holding AG
Source
NIDFSINVIMA
Roche Diagnostics Gmbh
Manufacturer Parent Company (2017)
Roche Holding AG
Source
NIDFSINVIMA
ROCHE DIAGNOSTICS GMBH || Importer: PRODUCTOS ROCHE S.A.
Manufacturer Parent Company (2017)
Roche Holding AG
Source
NIDFSINVIMA
ROCHE DIAGNOSTICS GMBH || Importer: PRODUCTOS ROCHE S.A
Manufacturer Parent Company (2017)
Roche Holding AG
Source
NIDFSINVIMA
55 more
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