RegWardenFDA facility compliance records
Recall

Class II — Cenorin, LLC

Recalling firmCENORIN
Registered facilityCENORIN, LLC (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonDryer unit not heating. Manufacturing issue causes the terminal block to overheat, char and/or burn.
ProductThermaSure(TM), a CENORIN(TM) product, SERIES 130 MEDICAL DEVICE DRYER: (a) Model 135; (b) Model 136 Forced air dryer for medical devices
Quantity34 units
DistributionWorldwide Distribution - US (Nationwide) Internationally to Japan, Hong Kong, Brunei, and Israel
Initiated2017-06-07
Classified2017-08-14
Terminated2018-05-02
Recall numberZ-3032-2017
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-3032-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/77637/

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