Abbott Laboratories: Medical Device Recall in 2023 - (Recall #: Z-0958-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels

Product Classification:

Class III

Date Initiated: November 24, 2022

Date Posted: January 25, 2023

Recall Number: Z-0958-2023

Event ID: 91303

Reason for Recall:

Reaction vessels may contain a potential contaminant that could affect their optical performance.

Status: Ongoing

Product Quantity: 70 cases

Code Information:

UDI-DI/Lots: 00380740129026/000586790 and 000586879

Distribution Pattern:

US Distribution: IL, MN, MO, NC, ND, NJ, NY, OK, SC, TX, WV

Voluntary or Mandated:

Voluntary: Firm initiated