RegWardenFDA facility compliance records
Recall

Class II — Mesa Laboratories, Inc.

Recalling firmMESA LABORATORIES, INC.
Registered facilityView this company's 4 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass II
StatusTerminated
ReasonMesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution due to mold growth.
ProductpH 7.0 Buffer Solution Pint and Quart Bottles, Part Number 02.0030 for Pints and 02.0031 for Quarts. Packaged in Plastic Bottles. Can be sold individually or in cartons with 6 bottles per box (for quart bottles only). Used in the hemodialysis setting to calibrate pH meters.
Quantity58,466 bottles
DistributionWorldwide Distribution-USA (nationwide) and the country of Canada.
Initiated2013-09-13
Classified2013-11-07
Terminated2016-08-08
Recall numberZ-0175-2014
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 — Mesa Laboratories, Inc. (Z-0175-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/66475/

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