Abbott Molecular, Inc.: Medical Device Recall in 2022 - (Recall #: Z-0461-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Alinity m System, Part No. 08N53-002

Product Classification:

Class II

Date Initiated: December 6, 2021

Date Posted: January 12, 2022

Recall Number: Z-0461-2022

Event ID: 89167

Reason for Recall:

There is a software issue associated with the ability to properly complete a Field Service Engineer Maintenance and Diagnostics procedure.

Status: Ongoing

Product Quantity: 742 devices

Code Information:

Alinity m System, Model 08N53-002, all serial numbers

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Brazil, Cambodia, Canada, Chile, Colombia, Czech Republic, Egypt, El Salvador, Estonia, Finland, France, Germany, Hong Kong, Ireland, Israel, Italy, Japan, Malawi, Malaysia, Mexico, Montenegro, Morocco, Mozambique, Netherlands, New Zealand, Norway, Pakistan, Poland, Portugal, Romania, Russia, Saudi Arabia, Singapore, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Uganda, United Kingdom, and Vietnam.

Voluntary or Mandated:

Voluntary: Firm initiated