Facility

MESA LABORATORIES, INC.

3 recall(s) on record — most severe on record: Class II.

Key facts

3recalls · worst Class II

1inspections · worst VAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	1720309
Establishment type	Manufacture Medical Device
Location	12100 W 6th Ave Denver, CO, US 80228
Registration status	Active · expires 2026
Parent company	MESA LABORATORIES, INC. (owner-operator 1720309)
Brand names	Conductivity Standard Solution

Activity by year

Recalls (3)
Inspections (1)

Devices registered here (1)

Solution-Test Standard-Conductivity, Dialysis
Product code FKH (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.5820

Recalls & enforcement

Class IITerminated2017-05-12
Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to failure to meet product specifications.
Class IITerminated2016-04-04
Product resistance has fallen outside of label claim within expiry.
Class IITerminated2013-09-13
Mesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution due to mold growth.

FDA inspections (1)

NAI2018-03-16
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “MESA LABORATORIES, INC. (FEI 1720309) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1720309-mesa-laboratories-inc/

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