Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph
Clinical Chemistry · 21 CFR 862.1120
Recent MDR events
2,392 adverse event reports on file
- ABL800 FLEXJul 31, 2026MalfunctionRadiometer Medical Aps3002807968-2026-00082
- RAPIDPoint 500e Blood Gas SystemJul 30, 2026MalfunctionSiemens Healthcare Diagnostics Inc.3002637618-2026-00088
- i-STAT EG7+ CartridgeJul 27, 2026MalfunctionAbbott Point Of Care Inc.2245578-2026-00147
- ABL800 FLEX AnalyzerJul 27, 2026MalfunctionRadiometer Medical Aps3002807968-2026-00080
- ABL800 FLEXJul 27, 2026MalfunctionRadiometer Medical Aps3002807968-2026-00081
- ABL90 FLEX ANALYZERJul 22, 2026MalfunctionRadiometer Medical Aps3002807968-2026-00079
- ABL800 FLEX ANALYZEREJul 21, 2026MalfunctionRadiometer Medical Aps3002807968-2026-00076
- ABL800 FLEXJul 21, 2026MalfunctionRadiometer Medical Aps3002807968-2026-00075
- GEM PREMIER 5000Jul 9, 2026MalfunctionInstrumentation Laboratory Co.1217183-2026-00013
- GEM PREMIER 5000Jul 9, 2026MalfunctionInstrumentation Laboratory Co.1217183-2026-00014
Event type breakdown
Recalls
184 recall events for this product code
- Instrumentation LaboratoryOpen, ClassifiedAug 6, 2026
GEM Premier 7000 with iQM3
The active ingredient concentration in the lysing bag solution of specific GEM Premier 7000 with iQM3 PAK lots did not meet established manufacturing specifications. The malfunction could result in delayed recognition and management of Co-Oximetry and total bilirubin abnormalities and their sequelae.
Z-2899-2026 · View FDA record ↗ - Instrumentation LaboratoryOpen, ClassifiedAug 6, 2026
GEM Premier 5000 PAK
The active ingredient concentration in the lysing bag solution of specific GEM Premier 5000 lots did not meet established manufacturing specifications. The malfunction could result in delayed recognition and management of Co-Oximetry and total bilirubin abnormalities and their sequelae.
Z-2900-2026 · View FDA record ↗ - Instrumentation LaboratoryOpen, ClassifiedJul 29, 2026
Brand Name: GEM Premier 5000
BCR wands that received a configuration update (released under Service Information No. 2026-07 on or after April 8, 2026) may assign patient results to an incorrect patient ID. The root cause is a race condition introduced when the "price check" feature was disabled to reduce excess current draw. This causes buffered data from a previous scan to be transmitted instead of the most recent scan, populating a prior patient ID instead of the current one. This can result in erroneous results being attributed to the wrong patient, potentially leading to inappropriate clinical management.
Z-2821-2026 · View FDA record ↗ - Instrumentation LaboratoryOpen, ClassifiedJul 29, 2026
Brand Name: GEM Premier 7000 with iQM3
BCR wands that received a configuration update (released under Service Information No. 2026-07 on or after April 8, 2026) may assign patient results to an incorrect patient ID. The root cause is a race condition introduced when the "price check" feature was disabled to reduce excess current draw. This causes buffered data from a previous scan to be transmitted instead of the most recent scan, populating a prior patient ID instead of the current one. This can result in erroneous results being attributed to the wrong patient, potentially leading to inappropriate clinical management.
Z-2822-2026 · View FDA record ↗ - Instrumentation LaboratoryOpen, ClassifiedJul 29, 2026
Brand Name: GEM Premier 5000
BCR wands that received a configuration update (released under Service Information No. 2026-07 on or after April 8, 2026) may assign patient results to an incorrect patient ID. The root cause is a race condition introduced when the "price check" feature was disabled to reduce excess current draw. This causes buffered data from a previous scan to be transmitted instead of the most recent scan, populating a prior patient ID instead of the current one. This can result in erroneous results being attributed to the wrong patient, potentially leading to inappropriate clinical management.
Z-2823-2026 · View FDA record ↗ - Instrumentation LaboratoryOpen, ClassifiedJul 29, 2026
Brand Name: GEM Premier 5000
BCR wands that received a configuration update (released under Service Information No. 2026-07 on or after April 8, 2026) may assign patient results to an incorrect patient ID. The root cause is a race condition introduced when the "price check" feature was disabled to reduce excess current draw. This causes buffered data from a previous scan to be transmitted instead of the most recent scan, populating a prior patient ID instead of the current one. This can result in erroneous results being attributed to the wrong patient, potentially leading to inappropriate clinical management.
Z-2824-2026 · View FDA record ↗ - Instrumentation LaboratoryOpen, ClassifiedJul 29, 2026
Brand Name: GEM Premier 5000
BCR wands that received a configuration update (released under Service Information No. 2026-07 on or after April 8, 2026) may assign patient results to an incorrect patient ID. The root cause is a race condition introduced when the "price check" feature was disabled to reduce excess current draw. This causes buffered data from a previous scan to be transmitted instead of the most recent scan, populating a prior patient ID instead of the current one. This can result in erroneous results being attributed to the wrong patient, potentially leading to inappropriate clinical management.
Z-2825-2026 · View FDA record ↗ - Instrumentation LaboratoryOpen, ClassifiedJul 29, 2026
Brand Name: GEM Premier 5000
BCR wands that received a configuration update (released under Service Information No. 2026-07 on or after April 8, 2026) may assign patient results to an incorrect patient ID. The root cause is a race condition introduced when the "price check" feature was disabled to reduce excess current draw. This causes buffered data from a previous scan to be transmitted instead of the most recent scan, populating a prior patient ID instead of the current one. This can result in erroneous results being attributed to the wrong patient, potentially leading to inappropriate clinical management.
Z-2826-2026 · View FDA record ↗ - Abbott Point Of Care Inc.Open, ClassifiedApr 29, 2026
i-STAT EG7+ cartridge;
Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26) cartridge lots in the U.S. marketplace may report higher than expected PCO2 and lower than expected pH results due to a manufacturing issue. A falsely high pCO2 together with a falsely low pH makes the blood gas appear as if the patient is in severe respiratory acidosis. If the clinician believes the values are real, it may trigger unnecessary or even harmful interventions such as unnecessary ventilator changes, unnecessary medications, potential harm from overcorrection, or delays in identifying true problems.
Z-1999-2026 · View FDA record ↗ - Abbott Point Of Care Inc.Open, ClassifiedApr 29, 2026
i-STAT EG6+ cartridge;
Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26) cartridge lots in the U.S. marketplace may report higher than expected PCO2 and lower than expected pH results due to a manufacturing issue. A falsely high pCO2 together with a falsely low pH makes the blood gas appear as if the patient is in severe respiratory acidosis. If the clinician believes the values are real, it may trigger unnecessary or even harmful interventions such as unnecessary ventilator changes, unnecessary medications, potential harm from overcorrection, or delays in identifying true problems.
Z-2000-2026 · View FDA record ↗
Registered firms
153 firms currently registered for this product code
Diamond Diagnostics Inc.
Budapest, HU
Siemens Healthcare Diagnostics Manufacturing Ltd
SUDBURY Suffolk, GB
Nova Biomedical Corporation
WALTHAM, MA, US
Radiometer Medical Aps
BROENSHOEJ Hovedstaden, DK
Elitechgroup Inc
LOGAN, UT, US
Siemens Healthcare Diagnostics Inc.
Tarrytown, NY, US
Abbott Point Of Care Inc.
Princeton, NJ, US
Instrumentation Laboratory Co.
Bedford, MA, US
Nova Biomedical Corporation
Billerica, MA, US
Roche Diagnostics International Ltd.
ROTKREUZ Zug, CH
Siemens Healthcare Diagnostics Inc
East Walpole, MA, US
Abbott Point Of Care Canada Limited
Ottawa Ontario, CA
Opti Medical Systems Inc.
ROSWELL, GA, US
Medica Corp.
BEDFORD, MA, US
510(k) clearances
188 clearances for this product code
- Radiometer Medicals ApsApr 10, 2026
K252207 · ABL90 FLEX PLUS System, safeCLINITUBES
- Abbott Point of Care, Inc.May 2, 2025
K244014 · i-STAT CG4+ cartridge with the i-STAT 1 System
- Radiometer Medicals ApsDec 13, 2024
K240998 · ABL90 FLEX PLUS System
- Abbott Point of Care, Inc.Oct 27, 2023
K230285 · i-STAT CG8+ cartridge with the i-STAT 1 System
- Nova Biomedical CorporationSep 29, 2023
K221900 · Stat Profile Prime Plus Analyzer System
- Abbott Point of Care, Inc.Sep 15, 2023
K223857 · i-STAT G3+ cartridge with the i-STAT 1 System
- Instrumentation Laboratory CompanyAug 10, 2023
K223608 · GEM Premier 7000 with IQM3
- Medica CorporationJan 27, 2023
K211559 · EasyStat 300