RegWardenFDA facility compliance records
Recall

Class II — Cenorin, LLC

Recalling firmCENORIN
Registered facilityCENORIN, LLC (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonThe temperature sensor/control system in the HLD Systems Model 610 may provide a false temperature reading. This caused the water to remain at ambient temperature throughout the pasteurization cycle rather than using hot water.
ProductHLD System, Model 610, Medical Device Cleaning and High Level Disinfection Washer/Pasteurizer.
Quantity25 HLD systems
DistributionWorldwide Distribution - US (nationwide): CA, DE, FL, MA, MI, NY, PA, TX, UT, WA, and WI and the countries of Uruguay and Taiwan.
Initiated2013-01-24
Classified2014-07-06
Terminated2015-02-10
Recall numberZ-1995-2014
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 — Cenorin, LLC (Z-1995-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/68580/

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