FDA Recall Terminated

Tosoh AIA-900 immunoassay Analyzer

Recall: Z-0485-2019 · Initiated September 28, 2018

Recall

Recall Number
Z-0485-2019
Event Number
81219
Firm
Tosoh Bioscience Inc
FEI Number
3005529799
Product Code
KHO
Status
Terminated
Root Cause
Software design
Initiated
September 28, 2018
Terminated
July 8, 2020
Address
3600 Gantz Rd, Grove City, OH, 43123-1895

Description

Tosoh AIA-900 immunoassay Analyzer

Reason

A software issue may cause the liquid volume detection entries for 2nd and 3rd reagent bottles to be overwritten with the data from the 1st reagent bottle. Tosoh has released software version 2.51 (or later) to fix the problem. This failure is mitigated by the hardware design. The consequence would be a slight delay in testing patient sample or reporting patient result.

Action

On September 28, 2018, the firm issued an Urgent Medical Device Recall letter to affected customers. Customers were informed of the software issue. The firm has released software version 2.51 (or later) which corrects the problem. Three analyzers were identified that do not have the most current software version and are at risk for the error: 10313605, 10503612, and 10634103. A field service engineer will be contacting customers with these units in their possession to schedule a service visit in order to upgrade those analyzers to the current version of the operating software. Immediate Actions to be taken by the Customer/User -Thoroughly review the content of this letter. -Complete and return the attached Acknowledgement Form. -File this notice with your laboratory records and forward this information to other supervisors or managers in your laboratory to ensure that they are aware of the potential issue. If you have obtained unexpected test results, delays in test result reporting, or received any complaints of illness or adverse events associated with the use of the analyzer, please contact Tosoh Technical Support 24 hours a day, seven days a week at (800) 248-6764. Should you have any questions regarding this medical device recall, please feel free to contact Bernadette O'Connell at (800) 248-6764 or by email at [email protected]. She will be available to answer any questions Monday - Friday, from 9:00 AM to 5:00 PM (PST).

Distribution

Distributed to accounts in GA and NY.

Quantity

3