Inpeco S.A. recalls
Every recall we track for Inpeco S.A. — 32 in all, from 2018–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Inpeco S.A. peaked in 2020 (19); 32 since 2017.
All FDA recall records for Inpeco S.A. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 1 | 1 | 0 | 2 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 1 | 18 | 0 | 19 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 5 | 1 | 0 | 6 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 4 | 0 | 4 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Inpeco S.A. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Inpeco S.A. recalls
14 shown- Lower riskMedical device
Inpeco S.A. recalls FlexLab (FLX); Version: FLX-217-40;
Inpeco recalls FlexLab version FLX-217-40 due to label mismatch causing test errors. Affected units have specific serial numbers. Contact Inpeco for remedy.
InpecoOct 30, 2025 - Lower riskMedical device
Inpeco S.A. recalls FlexLab X (FXX) System. Potassium Test System. in vitro diagnostic
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.
InpecoSep 3, 2025 - Lower riskMedical device
Inpeco S.A. recalls Roche Cobas 8000 and Cobas PRO Interface Module (CO8 IM)- IVD FlexLab Automation System -a modular system designed to
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.
RocheNov 3, 2023 - Use cautionMedical device
Inpeco S.A. recalls Storage and Retrieval Module (SRM)-Laboratory Automation system Brand names of the same product: FlexLab (FLX),
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.
InpecoMar 10, 2023 - Lower riskMedical device
Inpeco S.A. recalls FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2). (Different brand names of same product.)
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.
InpecoSep 10, 2021 - Lower riskMedical device
Inpeco S.A. recalls Accelerator a3600 system with Sysmex XN-9000/XN-9100 Interface Module (dual robot) FLX-290-10; FLX-290-20 and Track to
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.
InpecoAug 7, 2020 - Lower riskMedical device
Inpeco S.A. recalls Accelerator a3600 Automation System with the Aliquoter Module (Inpeco P/N FLX-212) The FlexLab (aka Accelerator a3600
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.
InpecoJul 14, 2020 - Lower riskMedical device
Inpeco S.A. recalls FlexLab Automation System used with the following Modules: High Volume Storage(P/N FLX-270, FLX-271, FLX-276, FLX-282,
Inpeco recalls FlexLab automation systems with specific modules due to potential sensor delays that could cause safety issues in lab settings.
InpecoApr 7, 2020 - Lower riskMedical device
Inpeco S.A. recalls Accelerator a3600 Automation System using the Aliquoter Module (Inpeco P/N FLX-212) - Product Usage: The systems
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.
InpecoApr 7, 2020 - Lower riskMedical device
Inpeco S.A. recalls Accelerator a3600 Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000
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.
InpecoApr 7, 2020 - Lower riskMedical device
Inpeco S.A. recalls Inpeco FlexLab, ARCHITECT cSystem c8000/c16000 Interface Module, Part Numbers: FLX-208-00, FLX-208-10 - Product Usage:
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.
InpecoApr 7, 2020 - Lower riskMedical device
Inpeco S.A. recalls Abbott Accelerator a3600 Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions:
Inpeco recalls Abbott Accelerator a3600 Centrifuge Module with specific firmware versions and serial numbers due to potential unbalanced loads that could damage the centrifuge.
InpecoApr 7, 2020 - Use cautionMedical device
Inpeco S.A. recalls FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) (same product) FlexLab, Accelerator a3600 and Aptio
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.
InpecoAug 24, 2018 - Lower riskMedical device
Inpeco S.A. recalls FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2), Laboratory Automation System
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.
InpecoFeb 13, 2018
Inpeco S.A. recall questions
How many recalls has Inpeco S.A. had?
32 recalls from Inpeco S.A. are on record with U.S. safety agencies, from 2018–2025.
What is the most recent Inpeco S.A. recall?
Inpeco S.A. recalls FlexLab (FLX); Version: FLX-217-40;, dated Oct 30, 2025. Every Inpeco S.A. recall is listed on this page, newest first.
What should I do if I have a recalled Inpeco S.A. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Inpeco S.A. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.