FDA Recall Terminated

ARIES System and ARIES M1 System

Recall: Z-2094-2017 · Initiated April 19, 2017

Recall

Recall Number
Z-2094-2017
Event Number
77052
Firm
Luminex Corporation
FEI Number
3002524000
Product Code
OOI
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
April 19, 2017
Terminated
October 20, 2017
Address
12212 Technology Blvd, Austin, TX, 78727-6101

Description

ARIES System and ARIES M1 System

Reason

The hand-held barcode scanner that is used as an accessory to enter ARIES cassette and specimen identifications on the ARIES Systems populates patient sample IDs with a previously scanned sample ID when entering orders into an ARIES instrument.

Action

A recall notification letter was sent out on April 19, 2017. Prior to the recall letter being sent, the recalling firm sent a Customer Advisory Notification on April 14, 2017. The firm is also adding an accountability form to the customer notifications in order to document the customer responses to ensure that we account for the estimated 15 distributed units. For further questions, please call (877) 785-2323.

Distribution

Worldwide Distribution - US Distribution and to the countries of Finland and China.

Quantity

15 units