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Recall

Class II — Chromsystems Instruments & Chemicals GmbH

Recalling firmCHROMSYSTEMS INSTRUMENTS & CHEMICALS GMBH
Registered facilityCHROMSYSTEMS INSTRUMENTS & CHEMICALS GMBH (the firm's only registered facility)
ClassificationClass II
StatusCompleted
ReasonControl lots may not meet stability criteria and could result in increased results of patient samples for cortisone.
ProductMassChrom Cortisol, Cortisone Saliva Control Level I, Order No. 0349 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.
Quantity880 vials
DistributionUS Nationwide distribution in the states of NC and NY.
Initiated2020-10-29
Classified2020-12-02
Recall numberZ-0522-2021
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Chromsystems Instruments & Chemicals GmbH (Z-0522-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/86699/

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