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Moderate Complexity i-STAT cartridge - FDA Warning Letter November 2022

Can organizations continue to use the Abbott cTnI moderate complexity i-STAT cartridge based on the warning letter issued by the FDA in November 2022?

Any examples are for illustrative purposes only.

The Joint Commission, as an accrediting agency, will follow the guidance from the FDA, CMS and CLIA regarding this issue.  CMS/CLIA has updated their FAQ on this topic and they have stated that facilities can continue to use the Abbott cTnI moderate complexity i-STAT cartridge.

The Joint Commission suggests that your organization continue to work with your CLIA laboratory director, risk manager and legal team to determine your further course of action.  We also recommend that you frequently check the FDA website which assigns complexity to tests.
Manual: Laboratory
Chapter: Quality System Assessment for Nonwaived Testing QSA
New or updated requirements last added: December 25, 2022. New or updated requirements may be based on revisions to current accreditation requirements, regulatory changes, and/or an updated interpretation in response to industry changes. Substantive changes to accreditation requirements are also published in the Perspective Newsletter that is available to all Joint Commission accredited organizations.
Last reviewed by Standards Interpretation: December 25, 2022 Represents the most recent date that the FAQ was reviewed (e.g. annual review).
This page was last updated on December 25, 2022 with update notes of: Reflects new or updated requirements Types of changes and an explanation of change type: Editorial changes only: Format changes only. No changes to content. | Review only, FAQ is current: Periodic review completed, no changes to content. | Reflects new or updated requirements: Changes represent new or revised requirements.
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