PerkinElmer Health Sciences Canada, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0513-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

PerkinElmer QSight 210 MD Mass Spectrometer Simplicity 3Q MD v1.0 with Hot Fix 2 Software intended to identify compounds in human samples by ionizing the compound and separating the resulting ions. Part Number: BC004872

Product Classification:

Class II

Date Initiated: September 24, 2018

Date Posted: December 5, 2018

Recall Number: Z-0513-2019

Event ID: 81266

Reason for Recall:

Under certain conditions when using PerkinElmer QSight 210 MD mass spectrometer with Simplicity 3Q MD and Hotfix 2 software, it is possible for the original data from the last acquired sample to be over-written when the automatic flush is enabled.

Status: Terminated

Product Quantity: 18 units

Code Information:

210MDBC709100008 210MD8C709140010 210MD8C709150009 210MDBC709160011 210MDBC709180012 210MDBC709200013 210MD8C710020014 210MDBC710050016 210MD8C710110018 210MDBC710170020 210MD8C710180022 210MD8C712220428 210MDBC801240030 210MDBC801250031 210MDBC802140032 210MD8C802150033 210MD8C802260035 210MDBC803190037

Distribution Pattern:

FL, MN, PA India, Italy, Korea, Spain

Voluntary or Mandated:

Voluntary: Firm initiated