UTAK LABORATORIES, I
1 recall(s) on record — most severe on record: Class III.
Recalls by year
- Recalls (1)
Registered facilities (1)
- UTAK LABORATORIES, INC. FEI 2022375 · CA
Recalls & enforcement
- Class IIITerminated2020-03-20The product has an incorrect reference value for cadmium and an incorrect expected range.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “UTAK LABORATORIES, I — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-2022375-utak-laboratories-i/
Alerts for UTAK LABORATORIES, I
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.