FDA recall record

Bio-Rad Laboratories EVOLIS Microplate System, Catalog # 89601 recall — FDA Z-0807-2016

The error "Washer Reagent Clean Fluid" level low alarmed, which prompted the customer to open the system drawer. When the system drawer was opened the…

Class IIclassification
Z-0807-2016official record ID
Feb 24, 2016report date

Recall record at a glance

Official recordZ-0807-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBio-Rad Laboratories, Inc.
Report dateFeb 24, 2016
Recall initiation dateDec 22, 2015
Quantity278 units
LocationRedmond, WA, United States

Official product description

EVOLIS Microplate System, Catalog # 89601. Part number 89788 for the EVOLIS Operator's Manual. in vitro diagnostic Product Usage: EVOLIS Microplate System is a 4 plate fully integrated microplate processing system designed for use with multiple EIA assays.

Why the product was recalled

The error "Washer Reagent Clean Fluid" level low alarmed, which prompted the customer to open the system drawer. When the system drawer was opened the customer noted the plate transport was still running and as a consequence the plate was pushed off the plate transporter.

Distribution information

US Nationwide Distribution including Puerto Rico.

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: Letter.

What to do next

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About this record

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