AB SCIEX 3200MD QTRAP¿ LC/MS/MS System Mass Spectrometer for In-Vitro… — Class II medical device recall Z-2527-2016

Terminated recall by Ab Sciex, reported 2016-08-24, distributed nationwide. MultiQuant MD software where under certain conditions a user can be presented with incorrect quantitative resu

Recall number	`Z-2527-2016`
Product type	Medical device
Classification	Class II
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	Ab Sciex, Framingham, MA, United States
Recall initiated	2016-06-16
Classified	2016-08-12
Reported by FDA	2016-08-24
Terminated	2017-03-02
Distributed	Nationwide (US)
Countries outside the US	AT, CA, CH, CN, DE, FR, GB, IE, IN, IT, KR, MY, NL, NO, RU, SG
Quantity	2 units
Reason classes	software
Model numbers	`3200MD`, `5024500`

Product

AB SCIEX 3200MD QTRAP¿ LC/MS/MS System Mass Spectrometer for In-Vitro Diagnostic Use. Instrument Part Number (REF): 5024500 3200MD series and 4500MD series are mass spectrometers intended to identify inorganic or organic compounds (e.g., lead, mercury, and drugs) in human specimens by ionizing the compound under investigation and separating the resulting ions by means of an electrical and magnetic field according to their mass. It is intended for in vitro diagnostic purposes. For in vitro diagnostic use.

Reason for recall

MultiQuant MD software where under certain conditions a user can be presented with incorrect quantitative results when using the Sum Multiple Ions feature.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2527-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.