# FDA recall Z-2333-2018

> **ECOLAB INC** · Class III · device recall initiated 2017-11-22.

## Product

ECOLAB MICROTEK Rolled Probe Cover, 2.6 cm x 20 cm (1 in x 8 in), Ref PC0906, packaged 1 probe cover/pouch, 25 pouches/carton, 2 cartons/shipping case, Sterile, RX.      To be used as a physical barrier for protection against the effects of environmental exposure (e.g. body fluids, gels) and/or to maintain the required hygienic level of various diagnostic or surgical procedures which utilize a transducer (probe).

## Reason for recall

The incorrect IFU was shipped with the product.

## Distribution

US Distribution to the states of : CA, IL, LA, SC, TX, and WI.  There was no foreign/government/military distribution.

## Key facts

- **Recall number:** Z-2333-2018
- **Recalling firm:** ECOLAB INC
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-11-22
- **Report date:** 2018-07-11
- **Termination date:** 2020-07-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Paul, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2333-2018

## Citation

> AI Analytics. FDA recall Z-2333-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2333-2018. Source: US FDA. Licensed CC0.

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