Glucose Dehydrogenase, Glucose
Clinical Chemistry · 21 CFR 862.1345
Recent MDR events
74,205 adverse event reports on file
- ACCU-CHEK ® INSTANTJul 31, 2026MalfunctionRoche Diabetes Care, Inc.3011393376-2026-00464
- ACCU-CHEK ® PERFORMAJul 31, 2026MalfunctionRoche Diabetes Care, Inc.3011393376-2026-00465
- ACCU-CHEK ® PERFORMAJul 31, 2026MalfunctionRoche Diabetes Care, Inc.3011393376-2026-00466
- ACCU-CHEK INFORM II TEST STRIPSJul 31, 2026MalfunctionRoche Diagnostics1823260-2026-03142
- ACCU-CHEK ® INSTANTJul 31, 2026MalfunctionRoche Diabetes Care, Inc.3011393376-2026-00467
- ACCU-CHEK ® INSTANTJul 30, 2026MalfunctionRoche Diabetes Care, Inc.3011393376-2026-00463
- ACCU-CHEK INFORM II TEST STRIPSJul 29, 2026MalfunctionRoche Diagnostics1823260-2026-03055
- ACCU-CHEK INFORM II TEST STRIPSJul 29, 2026MalfunctionRoche Diagnostics1823260-2026-03107
- ACCU-CHEK INFORM II TEST STRIPSJul 29, 2026MalfunctionRoche Diagnostics1823260-2026-03105
- ACCU-CHEK ® PERFORMAJul 28, 2026InjuryRoche Diabetes Care, Inc.3011393376-2026-00457
Event type breakdown
Product problems
Reported product problem codes, most common first
Trend for “Incorrect, Inadequate or Imprecise Result or Readings”
Recalls
51 recall events for this product code
- Roche Diabetes Care, Inc.TerminatedMay 9, 2018
Accu-Chek Aviva Plus Test Strip, Blood glucose monitoring system, Catalog nos. 06908217001, 06908268001, 06908349001,06908217001
The recalling firm identified four US lots of test strips out of specification. Affected strips show increased potential for strip errors prior to applying blood, strips not detected once inserted, or biased results, which may not be detectable. In the case of a biased result, incorrect action could be taken by the user in response to the displayed blood glucose result.
Z-2185-2018 · View FDA record ↗ - Roche Diabetes Care, Inc.TerminatedMay 9, 2018
Accu-Chek Performa Test Strip, Blood glucose monitoring system, Catalog no. 07299702001
The recalling firm has identified two lots of test strips that are out of specification. Affected test strips show an increased potential for: strip errors prior to applying a blood sample; strips not detected once inserted; or a biased result may occur, which may not be detectable. In the case of a biased result, incorrect action could be taken by the user in response to the displayed blood glucose result as compared to the actual blood glucose value.
Z-2186-2018 · View FDA record ↗ - Roche Diabetes Care, Inc.TerminatedMay 9, 2018
Accu-Chek Inform II Test Strip, Whole blood glucose test system, Catalog no. 05942861001
The recalling firm has identified two lots of test strips that are out of specification. Affected test strips show an increased potential for: strip errors prior to applying a blood sample; strips not detected once inserted; or a biased result may occur, which may not be detectable. In the case of a biased result, incorrect action could be taken by the user in response to the displayed blood glucose result as compared to the actual blood glucose value.
Z-2187-2018 · View FDA record ↗ - Roche Diagnostics Operations, Inc.TerminatedMar 14, 2016
Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System
Accu-Chek Inform II Base Unit might produce physical transmission errors in the form of data loss in the communication between the meter and the Data Management Systems (DMS). The issue can lead to the data loss or in the worst case to an erroneous assignment of the patient data (patient mismatch). The issue will only occur at sites using POTCT1-A communication via USB.
Z-1172-2016 · View FDA record ↗ - Lifescan IncTerminatedApr 2, 2012
OneTouch Verio IQ Blood Glucose Monitoring System Kit;
An error was discovered in the OneTouch IQ meter software so that the meter turns itself off when a user attempts to view results in the "Results Log" when the log has 256 or a multiple of 256 items to display.
Z-1359-2012 · View FDA record ↗ - Bayer Healthcare, LLCTerminatedSep 19, 2011
Contour, Contour TS Blood Glucose Test Strips and Bonus Packs
All 10- or 25- count glucose test strip vials, either loose vials or found in patient starter kits of Contour, Contour TS and Contour" USB blood glucose meters are being recalled a packaging issue which, under certain conditions, can cause some test strips packaged in some small-count vials to operate outside of US FDA-cleared performance specifications and produce a low-bias reading during blood
Z-3268-2011 · View FDA record ↗ - Roche Diagnostics Corp.TerminatedAug 11, 2009
Roche ACCU-Chek Active Meter Kit, Roche Diagnostics, Indianapolis, IN; REF 03184501001 includes the Roche ACCU-CHEK Softclix Lancing Device, Distributed by Roch
The lancet cap may be missing, which could result in an unintended lancet stick to the user.
Z-1591-2009 · View FDA record ↗ - Roche Diagnostics Corp.TerminatedAug 11, 2009
Roche ACCU-Chek Voicemate Meter, Roche Diagnostics, Indianapolis, IN; REF 12030802001 includes the Roche ACCU-CHEK Softclix Lancing Device, Distributed by Roche
The lancet cap may be missing, which could result in an unintended lancet stick to the user.
Z-1592-2009 · View FDA record ↗ - Roche Diagnostics Corp.TerminatedAug 11, 2009
Roche ACCU-Chek Aviva Meter Kit, Roche Diagnostics, Indianapolis, IN; REF 04893247001 includes the Roche ACCU-CHEK Softclix Lancing Device, Distributed by Roche
The lancet cap may be missing, which could result in an unintended lancet stick to the user.
Z-1593-2009 · View FDA record ↗ - Roche Diagnostics Corp.TerminatedAug 11, 2009
Roche ACCU-CHEK Compact Plus Meter Kit, Roche Diagnostics, Indianapolis, IN; REFS 03149137001, 05177294001 and 05079241001 include the Roche ACCU-CHEK Softclix
The lancet cap may be missing, which could result in an unintended lancet stick to the user.
Z-1595-2009 · View FDA record ↗
Registered firms
260 firms currently registered for this product code
Abbott Diabetes Care Inc.
ALAMEDA, CA, US
Trividia Health Taiwan, Inc.
HSINCHU CITY Hsinchu (City), TW
Phc Corporation
MIMA Tokushima, JP
Roche Diagnostics Gmbh
MANNHEIM Baden-Wurttemberg, DE
Ascensia Diabetes Care Holdings Ag
Basel Basel-Stadt, CH
Ascensia Diabetes Care Us Inc.
Parsippany, NJ, US
Phc Corporation
Chiyoda-ku Tokyo, JP
Pt Phc Indonesia
Cikarang Barat Bekasi Jawa Barat, ID
Lake County Press
Waukegan, IL, US
Nova Biomedical Corporation Diabetes Products
Billerica, MA, US
Bionostics, Inc.
Devens, MA, US
Ascensia Diabetes Care Poland Sp. Z O.o.
Warszawa Mazowieckie, PL
Flextronics Manufacturing Aguascalientes, S.a De C.v
Aguascalientes, MX
Andon Health Co., Ltd
TIANJIN, CN
Hmd Biomedical, Inc.
Hsinchu County, TW
Gl Diabetes Corporation
San Diego, CA, US
Abbott Ireland Diabetes Care
Donegal Town, IE
510(k) clearances
73 clearances for this product code
- Abott LaboratoriesSep 17, 2015
K152328 · FreeStyle InsuLinx Blood Glucose Monotioring System
- Roche Diagnostics CorporationDec 17, 2014
K142089 · ACCU-CHEK AVIVA EXPERT SYSTEM
- Eps Bio Technology Corp.Apr 28, 2014
K133537 · EGV1.1 SELF MONITORING BLOOD GLUCOSE SYSTEM AND EGV1.1 PRO MONITORING BLOOD GLUCOSE SYSTEM
- Ceragem Medisys, Inc.Feb 28, 2014
K131727 · CERA-CHEK 1070 BLOOD GLUCOSE MONITORING SYSTEM
- Roche Diagnostics Operations, Inc.Oct 11, 2013
K131366 · ACCU-CHEK AVIVA EXPERT BLOOD GLUCOSE MONITORING SYSTEM
- Nova Biomedical CorporationApr 4, 2013
K122688 · NOVA MAX MINI BLOOD GLUCOSE AND B-KETONE MONITOR
- Hmd Biomedical, Inc.Feb 14, 2013
K121433 · GOODLIFE CS-200 (SINGLE PATIENT USE), CS-200 PROFESSIONAL (MULTIPLE PATIENT USE) BLOOD GLUCOSE MONITORING SYSTEMS
- Nova Biomedical CorporationDec 20, 2012
K122435 · NOVA ONE BLOOD GLUCOSE MONITOR