RegWardenFDA facility compliance records
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
StatusTerminated
ReasonXXX
ProductMassChrom Amino Acid Analysis Plasma Control Level III, Order No. 0473 - Product Usage: The kit is intended for amino acid metabolic screening, confirmation of a tentative diagnosis, and monitoring of treatment in individuals diagnosed with a metabolic disorder.
Quantity342 vials
DistributionWorldwide distribution - US Nationwide distribution in the states of CA and NY; The countries of Australia, Belgium, Brazil, Germany, Finland, France, Greece, Israel, Italy, Canada, Croatia, Kuwait, Austria, Russia, Switzerland, South Africa, Taiwan, Turkey, and United Arab Emirates.
Initiated2020-11-02
Classified2020-12-04
Terminated2021-12-20
Recall numberZ-0539-2021
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-0539-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/86719/

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