FDA recall record

Beckman Coulter IRISpec CA/CB/CC control, Catalog #800-7211, containing 3 x 100 mL bottles recall — FDA Z-0984-2022

IRISpec CA failures for glucose.

Class IIIclassification
Z-0984-2022official record ID
Apr 27, 2022report date

Recall record at a glance

Official recordZ-0984-2022
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmBeckman Coulter, Inc.
Report dateApr 27, 2022
Recall initiation dateFeb 16, 2022
Quantity12,306 kits
LocationMiami, FL, United States

Official product description

Beckman Coulter IRISpec CA/CB/CC control, Catalog #800-7211, containing 3 x 100 mL bottles each of CA Control, CB Control, and CC Control.

Why the product was recalled

IRISpec CA failures for glucose.

Distribution information

Worldwide distribution - US Nationwide, including Puerto Rico and the countries of Brazil, Canada, Curacao, Guatemala, Mexico, Philippines, Singapore, and Taiwan.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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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