MESA LABORATORIES, INC.
3 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (3)
Registered facilities (4)
- Mesa Laboratories Bozeman Manufacturing Facility (Zoot) FEI 3013667284 · MT
- MESA LABORATORIES, INC. FEI 1720309 · CO
- IBP MEDICAL GMBH FEI 3003884198 · DE
- Mesa Germany GmbH FEI 3008925937 · DE
Recalls & enforcement
- Class IITerminated2017-05-12Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to failure to meet product specifications.
- Class IITerminated2016-04-04Product resistance has fallen outside of label claim within expiry.
- Class IITerminated2013-09-13Mesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution due to mold growth.
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. “MESA LABORATORIES, INC. — 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-1720309-mesa-laboratories-inc/
Alerts for MESA LABORATORIES, INC.
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.