FDA recall record

Roche Diagnostics Operations Tina-quant Complement C4 ver.2, Catalog 05991994190 recall — FDA Z-0103-2021

Roche has confirmed customer complaints of low quality (QC) recovery and invalid calibrations for the identified products. A discoloration (yellow color)…

Class IIIclassification
Z-0103-2021official record ID
Oct 21, 2020report date

Recall record at a glance

Official recordZ-0103-2021
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmRoche Diagnostics Operations, Inc.
Report dateOct 21, 2020
Recall initiation dateAug 27, 2020
Quantity180 units
LocationIndianapolis, IN, United States

Official product description

Tina-quant Complement C4 ver.2, Catalog 05991994190

Why the product was recalled

Roche has confirmed customer complaints of low quality (QC) recovery and invalid calibrations for the identified products. A discoloration (yellow color) was observed and is the result of cross contamination between the R1 and R3 reagents.

Distribution information

Domestic distribution nationwide.

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: N/A.

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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