Roche Diagnostics Corporation: Medical Device Recall in 2018 - (Recall #: Z-1269-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: December 18, 2017

Date Posted: April 4, 2018

Recall Number: Z-1269-2018

Event ID: 79074

Reason for Recall:

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

Status: Terminated

Product Quantity:

Code Information:

None

Distribution Pattern:

US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated