Ecolab — Class III medical device recall Z-0753-2017
Terminated recall by Ecolab Inc, reported 2016-12-21, distributed in CA, FL, MI, NJ, TX, UT, VA. The reason for the recall is that the inner carton box of the Rolled Probe Cover PC0907NB has the incorrect ex
| Recall number | Z-0753-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ecolab Inc, Saint Paul, MN, United States |
| Recall initiated | 2016-11-30 |
| Classified | 2016-12-14 |
| Reported by FDA | 2016-12-21 |
| Terminated | 2019-08-21 |
| Distributed | CA, FL, MI, NJ, TX, UT, VA |
| Reason classes | labeling |
Product
Ecolab, Microtek Rolled Probe Cover PC0907NB, Rx Only.
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0753-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.