RegWardenFDA facility compliance records
Recall

Class III — Ecolab Inc

Recalling firmEcolab Inc
Registered facilityView this company's 3 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass III
StatusTerminated
ReasonThe reason for the recall is that the inner carton box of the Rolled Probe Cover PC0907NB has the incorrect expiration date (2015-10-01) on the label while the individual pouch labels and outer shipper have the correct expiration date (2018-10-01). The manufacturing date was inadvertently used as the expiration date on the inner carton box labels.
ProductEcolab, Microtek Rolled Probe Cover PC0907NB, Rx Only.
Quantity40 cases (144 eaches per box)
DistributionUS Distribution to the states of : CA, FL, MI, NJ, TX, UT and VA..
Initiated2016-11-30
Classified2016-12-14
Terminated2019-08-21
Recall numberZ-0753-2017
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 III recall — Ecolab Inc (Z-0753-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/75826/

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