AB Sciex, LLC: Medical Device Recall in 2023 - (Recall #: Z-0039-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Citrine QTRAP Mass Spectrometer, Part Number 5063685

Product Classification:

Class II

Date Initiated: August 30, 2023

Date Posted: October 11, 2023

Recall Number: Z-0039-2024

Event ID: 92810

Reason for Recall:

In rare occasions, the combination of a leak of a highly flammable solvent at the ion source probe, and an electrical discharge may result in a flame on top of the probe and possible ejection of the electrode assembly from the probe. There is a risk to the patient/user, customer property, or environment because there is a potential for a health risk and property damage should the flame be left unattended. The failure causes a delay in patient results.

Status: Ongoing

Product Quantity: 10

Code Information:

UDI-DI: 00842365100540; Serial Numbers: DD250051901, DD250172009, DD250182009, DD230001804, DD250111910, DD250132004, DD250091909, DD250101910, DD250192010, CN10011707PT

Distribution Pattern:

US Nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated