FDA Recall Terminated

QUANTA-Lyser 240 IFA, Part #GS0242. The instrument is a fully automated, high-throughput, bench top system designed for clinical use to automate slide and reagent barcode reading, sample dilution and distribution, reagent pipetting and dispensing, slide and plate washing, dispensing slide mounting medium in the preparation for microscope analysis, and photometric measurement of microwell plates.

Recall: Z-1221-2018 · Initiated January 26, 2018

Recall

Recall Number
Z-1221-2018
Event Number
79380
Firm
Inova Diagnostics Incorporated
FEI Number
2026994
Product Code
JJE
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
January 26, 2018
Terminated
May 22, 2018
Address
9900 Old Grove Rd, San Diego, CA, 92131-1638

Description

QUANTA-Lyser 240 IFA, Part #GS0242. The instrument is a fully automated, high-throughput, bench top system designed for clinical use to automate slide and reagent barcode reading, sample dilution and distribution, reagent pipetting and dispensing, slide and plate washing, dispensing slide mounting medium in the preparation for microscope analysis, and photometric measurement of microwell plates.

Reason

The device power supply was not manufactured according to specification which can result in the loss of the protective grounding of the instrument.

Action

The letters were issued via email on January 26, 2018, informing the consignee of the issue and the actions to be taken. The response forms were requested to be completed and returned by February 23, 2018, indicating receipt of the notification and confirmation that the power supply has been replaced. The firm reported on February 23, 2018 that responses have been received from both consignees. For further questions, please call (858) 586-9900 x 1381.

Distribution

There was no U.S. distribution. Distribution was made to Panama and United Kingdom.

Quantity

1 instrument