# FDA recall Z-2115-2020

> **Inpeco S.A.** · Class II · device recall initiated 2020-04-07.

## Product

Accelerator a3600 Automation System used with the following Modules: High Volume Storage(P/N FLX-270, FLX-271, FLX-276, FLX-282, FLX-283), HSQ Interface Module (P/N FLX-274), Aliquoter Module (P/N FLX-209), Rack Output Module ROM400 (P/N FLX-289), XN-9000 Interface Module (P/N FLX-290), Advia 2120 LAS Interface Module (P/N FLX-219), Vertical Transportation Module (P/N FLX -204), Rack Input Module (P/N FLX-214), AUWi System Interface Module (P/N FLX-286), Track To Rack Interface Module (P/N FLX-295) - Product Usage: is a modular system 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 unified workstation.

## Reason for recall

The sensors which activate the safety switches may be affected by delayed activation.  In 1% of the cases, the response delay can be up to a maximum delay of 2 seconds, instead of 40ms  expected by design.

## Distribution

The products were distributed to the following US States:  IL and NY.

## Key facts

- **Recall number:** Z-2115-2020
- **Recalling firm:** Inpeco S.A.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-07
- **Report date:** 2020-06-03
- **Termination date:** 2024-06-13

- **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-2115-2020

## Citation

> AI Analytics. FDA recall Z-2115-2020. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-2115-2020. Source: US FDA. Licensed CC0.

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