System, Fibrinogen Determination
Hematology · 21 CFR 864.7340
Recent MDR events
6 adverse event reports on file
- DADE THROMBIN REAGENTOct 23, 2024MalfunctionSiemens Healthcare Diagnostics Products Gmbh9610806-2024-00046
- DADE® THROMBIN REAGENTJul 25, 2024MalfunctionSiemens Healthcare Diagnostics Products Gmbh9610806-2024-00021
- OWREN'S VERONAL BUFFERSep 14, 2021MalfunctionSiemens Healthcare Diagnostics Products Gmbh9610806-2021-00062
- MULTIFIBREN UApr 4, 2019MalfunctionSiemens Healthcare Diagnostics Products Gmbh9610806-2019-00042
- MULTIFIBRIN UJun 19, 2015MalfunctionSiemens Healthcare Diagnostics Products Gmbh9610806-2015-00013
- MULTIFIBRIN USep 18, 2007MalfunctionDade Behring Gmbh9610806-2007-00011
Event type breakdown
Most-reported manufacturers
Recalls
3 recall events for this product code
- Diagnostica Stago, Inc.Open, ClassifiedAug 28, 2025
STA - Fibrinogen 5. Model/Catalog Number: 00674.
Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in UFH and LMWH applications.
Z-2476-2025 · View FDA record ↗ - Fisher DiagnosticsTerminatedUnknown
Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30 Determinations), REF/Model 100650, UDI 00845275000863, IVD; --- Fisher Diagnostics, a di
An issue was discovered with the Pacific Hemostasis Fibrinogen Degradation Products (FDP) kit, list number 100650, lot 948546 and FDP Latex Reagent, list 100651, lot 890199. While the kit performs accurately at FDP concentrations greater than 20 g/ml, there is an observed reduction in sensitivity when FDP levels are less than 20 g/ml. This reduction in sensitivity has been tied to FDP Latex Reagent lot 890199 and may result in false negatives.
Z-2762-2017 · View FDA record ↗ - Fisher DiagnosticsTerminatedUnknown
Pacific Hemostasis FDP Latex Reagent, REF/Model Number 100651, UDI 00845275000870, 1 x 5 mL, IVD; --- Fisher Diagnostics, a division of Fisher Scientific Compan
An issue was discovered with the Pacific Hemostasis Fibrinogen Degradation Products (FDP) kit, list number 100650, lot 948546 and FDP Latex Reagent, list 100651, lot 890199. While the kit performs accurately at FDP concentrations greater than 20 g/ml, there is an observed reduction in sensitivity when FDP levels are less than 20 g/ml. This reduction in sensitivity has been tied to FDP Latex Reagent lot 890199 and may result in false negatives.
Z-2763-2017 · View FDA record ↗
Registered firms
21 firms currently registered for this product code
Diagnostica Stago, Inc.
PARSIPPANY, NJ, US
Siemens Healthcare Diagnostics Products Gmbh
MARBURG Hesse, DE
Instrumentation Laboratory Co.
ORANGEBURG, NY, US
Instrumentation Laboratory Co. - Devens
Devens, MA, US
Diagnostica Stago - Taverny
Taverny Val-d'Oise, FR
Tcoag Ireland Limited
BRAY Wicklow, IE
Fisher Diagnostics
MIDDLETOWN, VA, US
R2 Diagnostics, Inc.
SOUTH BEND, IN, US
Helena Laboratories, Corp.
BEAUMONT, TX, US
Instrumentation Laboratory Co.
Bedford, MA, US
510(k) clearances
28 clearances for this product code
- Instrumentation Laboratory (IL) Co.Jul 24, 2025
K251968 · HemosIL Fibrinogen-C; HemosIL Fibrinogen-C XL
- Instrumentation Laboratory CODec 27, 2007
K073367 · HEMOSIL FIBRINOGEN-C
- Dade Behring, Inc.Jun 29, 2005
K050928 · DADE THROMBIN REAGENT
- Sigma Diagnostics, Inc.Oct 9, 1997
K971858 · SIGMA DIAGNOSTICS FIBRINOGEN KIT (886A/887A)
- Panbio, Inc.May 21, 1997
K970189 · FIF TM
- Crestat Diagnostics, Inc.Apr 16, 1997
K965113 · N-ASSAY TIA FIBRINOGEN TEST KIT
- Behring Diagnostics, Inc.Apr 19, 1994
K934326 · MULTIFIBREN U
- Instrumentation Laboratory COAug 13, 1993
K931721 · IL TEST FIBRINOGEN-C