FDA recall Z-1269-2018

Roche Diagnostics Corporation · Class II · device

Product

Modular E 170 Analyzer: Immunoassay Chemistry Analyzer, Chemistry (Photometric, Discrete) for clinical use, Catalog Numbers: 03739040692, 03023109001, 05023599001, 05023572001, 03739040001 & 03023109973.

Reason for recall

Complaints have been received concerning questionable results on analyzers due to customers utilizing sample 13 mm tubes without tube adapters.

Distribution

US Nationwide

Key facts

Status
Terminated
Initiation date
2017-12-18
Report date
2018-04-04
Termination date
2019-04-09
Voluntary/Mandated
Voluntary: Firm initiated
Location
Indianapolis, IN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1269-2018