Ab Sciex: Medical Device Recall in 2014 - (Recall #: Z-2609-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

AB SCIEX API 3200MD" LC/MS/MS System with software: MultiQuantMD 3.0In vitro diagnostic to identify inorganic or organic compounds (e.g., lead, mercury, and drugs) in human specimens Part Number 5024543.

Product Classification:

Class II

Date Initiated: July 15, 2014

Date Posted: September 17, 2014

Recall Number: Z-2609-2014

Event ID: 68821

Reason for Recall:

Software- AB SCIEX API 3200MD LC/MS/MS SYSTEM with MultiQuantMD 3.0 software may provide incorrect data for patient diagnosis

Status: Terminated

Product Quantity: 6 units

Code Information:

Serial Numbers: BV20031308, BV20081311, BV20051310, BV20071311, BV20101401, BV20131401

Distribution Pattern:

FL, NC, OK, PA, TX

Voluntary or Mandated:

Voluntary: Firm initiated