CLASS III Device recall · Reported 21 Dec 2016 · FDA Enforcement Report

Microtek Rolled Probe Cover PC0907NB recalled by Ecolab

Ecolab is recalling Microtek Rolled Probe Cover PC0907NB, distributed in 7 states. The recall was initiated on 30 Nov 2016 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codes15302

Quantity recalled40 cases (144 eaches per box)

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0753-2017
FDA event ID: 75826
Recalling firm: Ecolab, Saint Paul, MN
Classification: Class III
Status: Terminated
Recall initiated: 30 Nov 2016
FDA classified: 14 Dec 2016
Reported: 21 Dec 2016
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

30 Nov 2016	Recall initiated by company
14 Dec 2016	Classified by FDA	+14 days
21 Dec 2016	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The 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.

Product as listed by the FDA

Ecolab, Microtek Rolled Probe Cover PC0907NB, Rx Only.

Where it was distributed

US Distribution to the states of : CA, FL, MI, NJ, TX, UT and VA..

California Florida Michigan New Jersey Texas Utah Virginia

Questions about this recall

Why was it recalled?

Which lots are affected?

15302

Where was it sold?

US Distribution to the states of : CA, FL, MI, NJ, TX, UT and VA..

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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