BioMerieux SA: Medical Device Recall in 2017 - (Recall #: Z-1200-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

VIDAS 3 software v. 1.1.4

Product Classification:

Class II

Date Initiated: January 11, 2017

Date Posted: February 22, 2017

Recall Number: Z-1200-2017

Event ID: 76281

Reason for Recall:

During development of the VIDAS 3 software version 1.2, some anomalies have been identified and observed to be already present in the current software version VIDAS 3 version 1.1.4. available in the field.

Status: Terminated

Product Quantity: 1161 units

Code Information:

REF: #412590, Lot: Software version 1.1.4

Distribution Pattern:

U.S.

Voluntary or Mandated:

Voluntary: Firm initiated