Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

High RiskFDA Device
Medical Devices/Diagnostic Equipment

AB Sciex, LLC: Mass Spectrometers Recalled for Fire and Component Ejection Risks

Agency Publication Date: October 5, 2023
Share:
Sign in to monitor this recall

Summary

AB Sciex, LLC is recalling 65 mass spectrometers, including API3200MD, 4500MD, and Citrine models, because a rare combination of solvent leaks and electrical discharges can cause a flame to erupt from the probe. This defect can also cause the electrode assembly to be forcefully ejected from the device. If left unattended, these flames could cause property damage or serious health risks, while the equipment failure leads to significant delays in patient diagnostic results.

Risk

A leak of highly flammable solvent near the ion source probe can ignite during an electrical discharge, creating an active fire on top of the probe and potentially shooting internal metal components out of the machine.

What You Should Do

  1. Locate the serial number and part number on your mass spectrometer to determine if your unit is affected. Affected API3200MD units (Part 4466230) have serial numbers EQ230011907, EQ230021911, and EQ230001901.
  2. Check your 4500MD Triple Quad (Part 5032522) for UDI-DI 00842365102049 and serial numbers such as EJ230051806PL, EJ230061807PL, and others ending in numbers like 1808 through 2305.
  3. Identify affected Citrine QTRAP (Part 5063685) and Citrine Triple Quad (Part 5063684) units by checking for serial numbers starting with DD or DE, such as DD250051901 or DE220001803PL.
  4. If your serial number matches the affected list, contact your healthcare provider or AB Sciex, LLC immediately to discuss safety precautions and necessary corrective actions for the device.
  5. For further information or to report issues, contact the manufacturer, AB Sciex, LLC, or call the FDA's medical device recall line at 1-888-463-6332 (1-888-INFO-FDA).

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer correction/instruction

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: API3200MD Mass Spectrometer
Model / REF:
Part Number 4466230
Lot Numbers:
EQ230011907
EQ230021911
EQ230001901
Product: 4500MD Triple Quad Mass Spectrometer
Model / REF:
Part Number 5032522
UDI-DI: 00842365102049
Lot Numbers:
EJ230051806PL
EJ230061807PL
EJ230071808
EJ230101810
EJ230111811
EJ230121811
EJ230141811
EJ230151812
EJ230161812
EJ230171901
EJ230181901
EJ230191901
EJ230211905
EJ230221908
EJ230231908
EJ230251909
EJ230271910
EJ230281910
EJ230311911
EJ230331912
EJ230362003
EJ230372003
EJ230392004
EJ230412009
EJ230422011
EJ230442012
EJ230452012
EJ230472101
EJ230482103
EJ230512105
EJ240012110
EJ240022111
EJ240052111
EJ240082207
EJ240092209
EJ240142307
EJ240132305
EJ240062201
Product: Citrine QTRAP Mass Spectrometer
Model / REF:
Part Number 5063685
UDI-DI: 00842365100540
Lot Numbers:
DD250051901
DD250172009
DD250182009
DD230001804
DD250111910
DD250132004
DD250091909
DD250101910
DD250192010
CN10011707PT
Product: Citrine Triple Quad Mass Spectrometer
Model / REF:
Part Number 5063684
UDI-DI: 00842365100533
Lot Numbers:
DE220001803PL
DE230011804
DE230031806
DE230041807
DE230051808
DE230071901
DE230081903
DE230091903
DE230162003
DE230272105
DE230292105
DE240002106
DE240022111
DE240042203

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92810
Status: Active
Manufacturer: AB Sciex, LLC
Sold By: AB Sciex, LLC
Manufactured In: United States
Units Affected: 4 products (3; 38; 10; 14)
Distributed To: Nationwide
Agency Last Updated: February 2, 2024

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.