Z-0581-2020 Class II Terminated

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

Recall Details

Product Type
Devices
Report Date
December 4, 2019
Initiation Date
September 23, 2019
Termination Date
July 6, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1432

Product Description

Atellica CH 930 Analyzer

Reason for Recall

Potential for calibration error resulting in QC failures after the calibration run with QC and patient results being 5 times higher.

Distribution Pattern

Distributed to accounts located in AL AZ AR CA CO FL GA IL IN IA KS KY LA MA MI MN MS NE NV NH NJ NM NY NC OH OR PA SC TN TX UT WA WV DC PR. Foreign distribution to AR AU AT BS BD BE BR BG CA CL CO CW CZ DK EG FI FR DE GR HU IN IR IE IL IT JP KW LV MY MX NL NG NO CN PK PH PL PT QA KR RO RU SA SG SK ZA ES SE CH TW TH TR AE GB UY VN.

Code Information

SMN 11067000, Software V1.20.0 and Lower, UDI 00630414002163