The Recall Desk

Manufacturer

Inpeco S.A.

33 recalls in our database name Inpeco S.A. as the manufacturing or recalling firm.

What the numbers show

Total
33
Critical
0
Severe
1
Most recent
2025-12-03

Of the 33 recalls from Inpeco S.A. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (3%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

26–33 of 33

  • HighFDA (Devices)·Z-2003-2020·2020-05-20

    Inpeco FlexLab Interface Module Recalled for Sample Cross-Contamination Risk

    Inpeco S.A. is recalling 82 FlexLab Interface Modules because a timeout error could cause sample cross-contamination.

    Product
    Inpeco FlexLab, ARCHITECT cSystem c8000/c16000 Interface Module, Part Numbers: FLX-208-00, FLX-208-10 - Product Usage: The FlexLab (aka Accelerator a3600) is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2004-2020·2020-05-20

    Inpeco Abbott Accelerator a3600 Interface Module Recalled for Cross-Contamination Risk

    Inpeco S.A. is recalling 273 Abbott Accelerator a3600 Interface Modules because a timeout error could cause sample cross-contamination.

    Product
    Abbott Accelerator a3600, ARCHITECT cSystem c8000/c16000 Interface Module, Part Numbers: ACP-208-00 - Product Usage: The FlexLab (aka Accelerator a3600) is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1888-2020·2020-05-13

    Inpeco Centrifuge Module Recall for Potential Unbalanced Load Damage

    Inpeco S.A. is recalling 23 Abbott Accelerator a3600 Centrifuge Modules because a loading algorithm defect may cause unbalanced loads that could damage the equipment.

    Product
    Abbott Accelerator a3600 Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86 or xCMd_2-5-0.elf and CM_1-7-1.H86 or xCMd_2-5-1-849fad9.elf
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-1887-2020·2020-05-13

    Inpeco FlexLab Centrifuge Module Recalled for Potential Load Imbalance

    Inpeco S.A. is recalling 65 FlexLab Centrifuge Modules because a tube loading algorithm defect may cause unbalanced loads that could damage the equipment.

    Product
    Inpeco FlexLab Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86 or xCMd_2-5-0.elf and CM_1-7-1.H86 or xCMd_2-5-1-849fad9.elf
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-1889-2020·2020-05-13

    Inpeco Siemens Aptio Centrifuge Module Recall for Tube Loading Algorithm Defect

    Inpeco S.A. is recalling 313 Siemens Aptio Automation Centrifuge Modules because a tube loading algorithm may cause unbalanced loads that could damage the centrifuge.

    Product
    Siemens Aptio Automation Centrifuge Module, tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86 or xCMd_2-5-0.elf and CM_1-7-1.H86 or xCMd_2-5-1-849fad9.elf
    Category
    Medical Device
    Distribution
    27 states
  • HighFDA (Devices)·Z-0361-2019·2018-11-07

    Inpeco FlexLab and Accelerator a3600 Recalled for Missing Safety Labels

    Inpeco S.A. is recalling 679 laboratory automation systems because some modules are missing safety pacemaker labels. The recall addresses a risk of pacemaker malfunction for personnel working near the equipment.

    Product
    FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) (same product) FlexLab, Accelerator a3600 and Aptio Automation are modular systems designed to automate Pre- Analytical and Post-Analytical processing,
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1798-2018·2018-05-16

    Inpeco Laboratory Automation Systems Recalled for Module Freezing Risk

    Inpeco S.A. is recalling 18 laboratory automation systems because a module may freeze without warning, potentially delaying patient test results.

    Product
    FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2), Laboratory Automation System
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0587-2017·2016-11-23

    Inpeco Laboratory Automation Systems Recalled for Burnt Sockets

    Inpeco is recalling FlexLab, Accelerator a3600, and Aptio Automation systems because field reports indicate burnt Schuko sockets and smoke.

    Product
    FlexLab, Accelerator a3600 and Aptio Automation are modular systems designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The systems consolidate multiple Analytical instruments into a unifie
    Category
    Medical Device
    Distribution
    2 states