RegWardenFDA facility compliance records
Recall

Class II — Sunstar Americas, Inc.

Recalling firmSunstar Americas, Inc.
Registered facilitySUNSTAR AMERICAS, INC. (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonProduct lacks premarket clearance.
ProductBUTLER Clear Dip, 12 bottles/case
Quantity22514 ea
DistributionUnited States Nationwide distribution.
Initiated2022-01-14
Classified2022-03-03
Terminated2023-08-28
Recall numberZ-0720-2022
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 — Sunstar Americas, Inc. (Z-0720-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/89460/

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