Every recall we track for Inpeco S.A. — 32 in all — plus the complaints and injury reports the public filed about them.
Inpeco recalls FlexLab (FLX-217-10) units where mismatched labels on sample tubes may cause delayed or incorrect lab results. Affected units have specific serial numbers and were sold with certain software versions.
Inpeco recalls FlexLab version FLX-217-40 due to label mismatch causing test errors. Affected units have specific serial numbers. Contact Inpeco for remedy.
Inpeco recalls FlexLab Potassium Test System due to untested safety of blood sample analysis function. This may cause inaccurate test results or delayed patient care. Affected units have specific serial numbers and part numbers.
Inpeco recalls FlexLab X Potassium Test System due to unverified safety of blood test results. This may cause inaccurate patient results or delays in treatment.
Roche recalls Cobas 8000 and Cobas PRO Interface Modules with firmware versions COBASa_2.2.0 and COBASa_2.3.0 due to potential delayed sample tube processing. Affected units include specific hardware and serial numbers.
Inpeco recalls Alinity h Interface Module (HSQ) lab automation systems due to potential mis-association of sample IDs causing incorrect electrolyte results. This could lead to improper treatment or serious health risks if not corrected.
Inpeco recalls FlexLab and Accelerator laboratory automation systems due to firmware that may cause incorrect electrolyte test results, potentially leading to serious health issues if not corrected.
Inpeco recalls Vesmatic Cube 80 Interface Modules that may mis-associate sample IDs causing incorrect electrolyte results. This could lead to inappropriate treatment or failure to treat abnormal results, risking serious health issues including cardiac arrhythmias and death.
Inpeco recalls FlexLab IOM systems with firmware versions prior to 2-3-0 on GWC boards and all versions on DDT boards due to potential misidentification of sample tubes, which could lead to incorrect electrolyte results and serious health risks.
Inpeco recalls FlexLab and related lab automation systems due to firmware issues that may cause incorrect electrolyte test results, potentially leading to serious health risks if not addressed.
Inpeco recalls FlexLab, Accelerator a3600, and Aptio Automation systems due to firmware issues causing incorrect patient test results. Affected units include specific serial numbers and part numbers.
Inpeco recalls FlexLab interface modules for Sysmex XN-9000/XN-9100 analyzers due to potential mis-association of sample IDs causing incorrect or delayed lab results. Affected units have specific serial numbers.
Inpeco recalls Aptio Automation systems with Sysmex XN-9000/XN-9100 Interface Modules due to potential mis-association of sample IDs, which could lead to incorrect or delayed lab results. Affected units have specific serial numbers.
Inpeco recalls Accelerator a3600 systems with Sysmex XN-9000/XN-9100 Interface Modules that may mis-associate sample IDs, causing incorrect or delayed lab results. Affected units have specific serial numbers.
Inpeco recalls FlexLab automation systems with Aliquoter Module (FLX-212) due to potential diluted samples causing inaccurate lab test results. Affected units have specific firmware versions and serial numbers.
Inpeco recalls Aptio Automation System with Aliquoter Module (FLX-212) due to clot detection errors causing diluted samples that may lead to incorrect test results. Affected units have specific serial numbers and firmware versions.
Inpeco recalls Accelerator a3600 Automation Systems with Aliquoter Module (FLX-212) that may dilute samples during error handling, leading to inaccurate lab test results. Affected units have specific firmware versions and serial numbers.
Inpeco recalls FlexLab Centrifuge Module (FLX-202) with specific firmware versions and serial numbers due to potential unbalanced loads that could damage the centrifuge.
Inpeco recalls Aptio Automation System interface modules due to communication errors causing sample tube misassociation. Affected units include specific model numbers and serial ranges. No remedy provided in official notice.
Inpeco recalls Accelerator a3600 Automation Systems with specific modules due to potential sensor delays that could cause safety issues. Affected units include models FLX-270 to FLX-295 with serial numbers ACP.050 and ACP.146.
Inpeco recalls FlexLab automation systems with specific modules due to potential sensor delays that could cause safety issues in lab settings.
Inpeco recalls specific Abbott Accelerator a3600 interface modules (serial numbers ACP.001-ACP.442) due to potential cross contamination if sample carousel lid remains open or manual processing takes too long.
Inpeco recalls FlexLab Augmentation System with Aliquoter Module (FLX-212) due to potential sample dilution causing inaccurate patient results. Affected units have specific serial numbers.
Inpeco recalls Aptio Automation System units with Aliquoter Module (P/N FLX-212) due to clot detection errors causing sample dilution with hydraulic water. Affected units have specific serial numbers listed in the recall.
Inpeco recalls FlexLab Automation System interface modules due to communication errors causing sample tube misassociation. Affected units include specific models and serial numbers listed in the recall notice.
Inpeco recalls Siemens Aptio Centrifuge Module (FLX-202) with specific firmware versions due to unbalanced loads that could damage the centrifuge.
Inpeco recalls Accelerator a3600 Automation Systems with Aliquoter Module (P/N FLX-212) due to clot detection errors causing sample dilution. Affected units have specific serial numbers.
Inpeco recalls Accelerator a3600 Automation System with specific interface modules due to a communication error causing sample tube misassociation. Affected units may require correction to prevent sample handling errors.
Inpeco recalls specific FlexLab interface modules that may cause sample cross contamination if the carousel lid stays open or manual processing takes too long. Affected units include part numbers FLX-208-00 and FLX-208-10 with serial numbers listed.
Inpeco recalls Abbott Accelerator a3600 Centrifuge Module with specific firmware versions and serial numbers due to potential unbalanced loads that could damage the centrifuge.
Inpeco recalls FlexLab, Accelerator a3600 and Aptio Automation modular systems due to missing safety pacemaker labels. People with pacemakers must maintain 200mm distance from modules to avoid malfunction.
Inpeco recalls specific lab equipment models due to potential freezing of modules without warning, which may delay test results for patients. Affected units include FlexLab (FLX), Accelerator a3600 (ACP), and Aptio Automation (AP2) with listed serial numbers.
