# FDA recall Z-1798-2018

> **Inpeco S.A.** · Class II · device recall initiated 2018-02-13.

## Product

FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2), Laboratory Automation System

## Reason for recall

Module may freeze without generating user warning. There is a potential risk in delay of sample processing, leading to delayed delivery of test results to patients.

## Distribution

Distributors in 2 states: NY and IL.

## Key facts

- **Recall number:** Z-1798-2018
- **Recalling firm:** Inpeco S.A.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-02-13
- **Report date:** 2018-05-16
- **Termination date:** 2019-04-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lugano, N/A, Switzerland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1798-2018

## Citation

> AI Analytics. FDA recall Z-1798-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-1798-2018. Source: US FDA. Licensed CC0.

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