Inpeco S.A.: Medical Device Recall in 2020 - (Recall #: Z-2141-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Accelerator a3600 Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000 Interface Module (P/N FLX-226-01, FLX-226-10), or StaRRsed Interface Module (P/N FLX-268-00) 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.

Product Classification:

Class II

Date Initiated: April 7, 2020

Date Posted: June 3, 2020

Recall Number: Z-2141-2020

Event ID: 85444

Reason for Recall:

The identified problem is an erroneous association between the carrier and the sample tube caused by a communication error between the firmware of the Interface Modules and the Automation software. This problem can occur only when one of these Interface Modules is put off-line after a carrier in their secondary lane is physically returned on the main track and then put back on-line when the carrier is used to transport another tube.

Status: Terminated

Product Quantity: 3 systems

Code Information:

Serial Numbers: ACP.290 ACP.343 ACP.365

Distribution Pattern:

US Nationwide including in the states of IL, NY.

Voluntary or Mandated:

Voluntary: Firm initiated