Inpeco S.A.: Medical Device Recall in 2018 - (Recall #: Z-1798-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: February 13, 2018

Date Posted: May 16, 2018

Recall Number: Z-1798-2018

Event ID: 79645

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.

Status: Terminated

Product Quantity: 18

Code Information:

Serial Numbers: Accelerator a3600 - ACP.150 ACP.185 ACP.186 ACP.192 ACP.202 ACP.214 FlexLab - FLX.0165 FLX.0127 FLX.0128 FLX.0133 FLX.0157 FLX.0160 FLX.0181 Aptio Automation - AP2.0054 AP2.0056 AP2.0060 AP2.0078 AP2.0095 Part Numbers of impacted sample tube carriers: 721501001 for 43 mm carriers, and 0A00006957 for 40 mm carriers

Distribution Pattern:

Distributors in 2 states: NY and IL.

Voluntary or Mandated:

Voluntary: Firm initiated