Z-1685-2018 Class II Terminated

Recalled by Siemens Healthcare Diagnostics, Inc. — Tarrytown, NY

Recall Details

Product Type
Devices
Report Date
May 16, 2018
Initiation Date
January 2, 2018
Termination Date
February 10, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
N/A

Product Description

IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi TG

Reason for Recall

Concentrations for the level of biotin that does not interfere is not currently listed in the instruction for use for the Dimension Vista CTNI, Dimension Vista MMB, Dimension Sirolimus, ADVIA Centaur FOL, ADVIA Centaur aHBcM and the following IMMULITE assays, 3gAllergy Specific IgE, anti-HBc, BR-MA (CA15-3), CEA, Folic Acid, Gastrin, OM-MA (CA125), Thyroglobulin, and Vitamin B12, and these assays are susceptible to interference from biotin.

Distribution Pattern

Nationwide and Canada, Mexico, and Thailand

Code Information

TG, TG (IMMULITE/IMMULITE 1000, LKTY1(D)), (IMMULITE 2000/IMMULITE 2000 XPi, LKTY2(D)) Lot codes: TG Lot # 346 347 348 349 350 351 352 353 354 355 356 D348 D349 D350 D351 D352 D353 D354 D356