---
title: "Inpeco S.A. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search Inpeco S.A. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/inpeco-s-a/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# Inpeco S.A. recall records

**10** reported ongoing

10 records in this archive. Latest source date Oct 30, 2025.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## Records and reported status

Oct 30, 2025 FDA device enforcement

### [FlexLab (FLX); Version: FLX-217-10;](https://isitonrecall.com/recall/fda-device-z-0595-2026-flexlab-flx-version-flx-217-10/)

The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results. This error occurs if the operators open the printer head of mALX to perform error recoveries o...

Class II Reported ongoing

Distribution: US Domestic: MI. OUS International: Australia, Finland, France, Germany, Italy, Portugal, Spain, and UK.

[Official source for FlexLab (FLX); Version: FLX-217-10;](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0595-2026%22)

Oct 30, 2025 FDA device enforcement

### [FlexLab (FLX); Version: FLX-217-40;](https://isitonrecall.com/recall/fda-device-z-0596-2026-flexlab-flx-version-flx-217-40/)

The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results, this error occurs if the operators open the printer head of mALX to perform error recoveries o...

Class II Reported ongoing

Distribution: US Domestic: MI. OUS International: Australia, Finland, France, Germany, Italy, Portugal, Spain, and UK.

[Official source for FlexLab (FLX); Version: FLX-217-40;](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0596-2026%22)

Sep 3, 2025 FDA device enforcement

### [FlexLab (FLX) System. Potassium Test System. in vitro diagnostic](https://isitonrecall.com/recall/fda-device-z-0106-2026-flexlab-flx-system-potassium-test-system-in-vitro-diagnostic/)

The FlexLab System Sample Integrity Module (SIM) includes function that determines the hemolysis, icterus, and lipemia (HIL) in blood samples. This function has not been evaluated for safety and effectiveness by the FDA, so its use may cause an increase in ...

Class II Reported ongoing

Distribution: US distribution to CA & NY.

[Official source for FlexLab (FLX) System. Potassium Test System. in vitro diagnostic](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0106-2026%22)

Sep 3, 2025 FDA device enforcement

### [FlexLab X (FXX) System. Potassium Test System. in vitro diagnostic](https://isitonrecall.com/recall/fda-device-z-0107-2026-flexlab-x-fxx-system-potassium-test-system-in-vitro-diagnostic/)

The FlexLab X System Sample Integrity Module (SIM) includes function that determines the hemolysis, icterus, and lipemia (HIL) in blood samples. This function has not been evaluated for safety and effectiveness by the FDA, so its use may cause an increase i...

Class II Reported ongoing

Distribution: US distribution to CA & NY.

[Official source for FlexLab X (FXX) System. Potassium Test System. in vitro diagnostic](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0107-2026%22)

Nov 3, 2023 FDA device enforcement

### [Roche Cobas 8000 and Cobas PRO Interface Module (CO8 IM)- IVD FlexLab Automation System -a modular system designed to automate Pre-Analytical and Post-Analytical processing, sam...](https://isitonrecall.com/recall/fda-device-z-0560-2024-roche-cobas-8000-and-cobas-pro-interface-module-co8-im-ivd-flexlab-automation-system-a-modular-syste/)

Firmware of the Interface Module with Roche Cobas 8000 and Cobas PRO (CO8 IM) may lead to a delayed sample tube processing.

Class II Reported ongoing

Distribution: Worldwide - US Nationwide distribution in the state of MA and the countries of AUSTRIA, BELGIUM, DENMARK, ITALY, NORWAY, SPAIN.

[Official source for Roche Cobas 8000 and Cobas PRO Interface Module (CO8 IM)- IVD FlexLab Automation System -a modula...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0560-2024%22)

Mar 10, 2023 FDA device enforcement

### [Input Output Module (IOM) FLX-201-Laboratory Automation system Brand names of the same product: FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) Part Numbers: FLX-...](https://isitonrecall.com/recall/fda-device-z-1559-2023-input-output-module-iom-flx-201-laboratory-automation-system-brand-names-of-the-same-product-flexlab/)

Firmware versions have the potential to mis-associate sample IDs leading to incorrect results or delayed sodium, potassium, and chloride patient results. Falsely increased or decreased electrolytes can lead to either inappropriate treatment of normal result...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, BRAZIL, CANADA, CHILE, CHINA, COLOMBIA, CZECH REPUBLIC, DENMARK, EAU, EGYPT, ...

[Official source for Input Output Module (IOM) FLX-201-Laboratory Automation system Brand names of the same product: F...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1559-2023%22)

Mar 10, 2023 FDA device enforcement

### [Storage and Retrieval Module (SRM)-Laboratory Automation system Brand names of the same product: FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) Part Numbers: ACP...](https://isitonrecall.com/recall/fda-device-z-1560-2023-storage-and-retrieval-module-srm-laboratory-automation-system-brand-names-of-the-same-product-flexla/)

Firmware versions have the potential to mis-associate sample IDs leading to incorrect results or delayed sodium, potassium, and chloride patient results. Falsely increased or decreased electrolytes can lead to either inappropriate treatment of normal result...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, BRAZIL, CANADA, CHILE, CHINA, COLOMBIA, CZECH REPUBLIC, DENMARK, EAU, EGYPT, ...

[Official source for Storage and Retrieval Module (SRM)-Laboratory Automation system Brand names of the same product: ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1560-2023%22)

Mar 10, 2023 FDA device enforcement

### [PVT Interface Module (PVT)-Laboratory Automation system Brand names of the same product: FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) Part Numbers: 72747000.A](https://isitonrecall.com/recall/fda-device-z-1561-2023-pvt-interface-module-pvt-laboratory-automation-system-brand-names-of-the-same-product-flexlab-flx-ac/)

Firmware versions have the potential to mis-associate sample IDs leading to incorrect results or delayed sodium, potassium, and chloride patient results. Falsely increased or decreased electrolytes can lead to either inappropriate treatment of normal result...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, BRAZIL, CANADA, CHILE, CHINA, COLOMBIA, CZECH REPUBLIC, DENMARK, EAU, EGYPT, ...

[Official source for PVT Interface Module (PVT)-Laboratory Automation system Brand names of the same product: FlexLab ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1561-2023%22)

Mar 10, 2023 FDA device enforcement

### [Vesmatic Cube 80 Interface Module (VMC)-Laboratory Automation system Brand names of the same product: FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) Part Numbers...](https://isitonrecall.com/recall/fda-device-z-1562-2023-vesmatic-cube-80-interface-module-vmc-laboratory-automation-system-brand-names-of-the-same-product-f/)

Firmware versions have the potential to mis-associate sample IDs leading to incorrect results or delayed sodium, potassium, and chloride patient results. Falsely increased or decreased electrolytes can lead to either inappropriate treatment of normal result...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, BRAZIL, CANADA, CHILE, CHINA, COLOMBIA, CZECH REPUBLIC, DENMARK, EAU, EGYPT, ...

[Official source for Vesmatic Cube 80 Interface Module (VMC)-Laboratory Automation system Brand names of the same prod...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1562-2023%22)

Mar 10, 2023 FDA device enforcement

### [Alinity h Interface Module (HSQ)-Laboratory Automation system Brand names of the same product: FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) Part Numbers: FLX-2...](https://isitonrecall.com/recall/fda-device-z-1563-2023-alinity-h-interface-module-hsq-laboratory-automation-system-brand-names-of-the-same-product-flexlab/)

Firmware versions have the potential to mis-associate sample IDs leading to incorrect results or delayed sodium, potassium, and chloride patient results. Falsely increased or decreased electrolytes can lead to either inappropriate treatment of normal result...

Class II Reported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, BRAZIL, CANADA, CHILE, CHINA, COLOMBIA, CZECH REPUBLIC, DENMARK, EAU, EGYPT, ...

[Official source for Alinity h Interface Module (HSQ)-Laboratory Automation system Brand names of the same product: Fl...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1563-2023%22)

## Reasons in these listed records

- The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results. This error occurs if the operators open the printer head of mALX to perform error recoveries or maintenance proced...
- The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results, this error occurs if the operators open the printer head of mALX to perform error recoveries or maintenance proced...
- The FlexLab System Sample Integrity Module (SIM) includes function that determines the hemolysis, icterus, and lipemia (HIL) in blood samples. This function has not been evaluated for safety and effectiveness by the FDA, so its use may cause an increase in erroneous results or...
- The FlexLab X System Sample Integrity Module (SIM) includes function that determines the hemolysis, icterus, and lipemia (HIL) in blood samples. This function has not been evaluated for safety and effectiveness by the FDA, so its use may cause an increase in erroneous results ...

These examples come from this result page and are not a ranking of every recall reason.

## Checking Inpeco S.A.

### Is there a recall on inpeco s.a. right now?

This archive contains 10 records, including 10 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

[Search Inpeco S.A.](https://isitonrecall.com/check/?q=Inpeco%20S.A.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
