Abbott Laboratories, Inc: Medical Device Recall in 2017 - (Recall #: Z-0166-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Tubing, Peristaltic Head Part Number 7-35009685-01 for use in clinical chemistry systems.

Product Classification:

Class II

Date Initiated: September 29, 2017

Date Posted: November 29, 2017

Recall Number: Z-0166-2018

Event ID: 78225

Reason for Recall:

The Peristaltic Head tubing placed on the ARCHITECT c4000, c8000, and c16000 has the possibility to leak due to a manufacturing issue associated with the tubing connector.

Status: Completed

Product Quantity: 44 units

Code Information:

Serial numbers - 125589-1-2, 125589-1-4

Distribution Pattern:

Worldwide distribution to US, Canada, France, and Germany.

Voluntary or Mandated:

Voluntary: Firm initiated