FDA recall record

Beckman Coulter Access Thyroglobulin Calibrators recall — FDA Z-0100-2024

It has been determined through an internal investigation that the alternate Access Thyroglobulin calibrator cards for use with the Thyg reagent packs…

Class IIclassification
Z-0100-2024official record ID
Oct 18, 2023report date

Recall record at a glance

Official recordZ-0100-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBeckman Coulter, Inc.
Report dateOct 18, 2023
Recall initiation dateJul 6, 2023
Quantity5980 units
LocationChaska, MN, United States

Official product description

Access Thyroglobulin Calibrators

Why the product was recalled

It has been determined through an internal investigation that the alternate Access Thyroglobulin calibrator cards for use with the Thyg reagent packs distributed in April 2023 will cause a decrease of approximately 11% in patient results.

Distribution information

worldwide except US, Canada, and China

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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