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Luminex Corporation recalls ARIES System and ARIES M1 System
Recalled May 24, 2017 · FDA recall Z-2094-2017 · Luminex
Hazard
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. · FDA Class II
Units
15 units
Sold at
Worldwide Distribution - US Distribution and to the countries of Finland and China.
Description
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.
Product
ARIES System and ARIES M1 System
Manufacturer(s)
Luminex Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →