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Open, Classified

VITROS Immunodiagnostic Products Troponin I ES Calibrators

FDA Recall Z-2358-2023 · Posted 2023-08-08

Recall StatusOpen, Classified
Product CodeMMI
Date Initiated2023-06-05
Product Quantity4,013 units

Reason for Recall

Reagent packs could potentially contain incorrect wells, which will generate incorrect, and potentially false negative, results.

Firm Action

Customers were sent a recall notification by mail dated 06/05/2023. The notification that customers immediately discontinue use of affected devices and discard any remaining inventory. Any discarded product will be replaced by QuidelOrtho or credit will be provided. Customers are asked to return the provided Confirmation of Receipt Form no later than 06/12/2023. If affected devices were further distributed customers are asked to forward the provided notification to those downstream customers. This notice is to be posted by all VITROS Systems until the expiration of affected devices, which is 06/10/2023. Customers with any questions may contact Quidel Ortho at 1-800-421-3311.

Root Cause

Process control

Distribution Pattern

Worldwide distribution - US Nationwide and the country of Canada.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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