# FDA recall Z-1847-2021

> **CooperSurgical, Inc.** · Class II · device recall initiated 2021-04-30.

## Product

CooperSurgical Wallach Loop Electrode 10mm x 10mm Square  P/N: 909131.  Disposable Universal Electrodes, LOOP electrodes, used for electro-excisional procedures, and for electro-fulguration procedures of the lower genital tract

## Reason for recall

The affected Wallach LOOP Electrodes were incorrectly packaged with a Round Electrode inside a package labeled as a Square Electrode.

## Distribution

US distribution to: CA, MD, MO, NJ, PA, and TX

## Key facts

- **Recall number:** Z-1847-2021
- **Recalling firm:** CooperSurgical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-04-30
- **Report date:** 2021-06-16
- **Termination date:** 2023-07-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Trumbull, CT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1847-2021

## Citation

> AI Analytics. FDA recall Z-1847-2021. Retrieved 2026-07-04 from https://api.ai-analytics.org/recall/Z-1847-2021. Source: US FDA. Licensed CC0.

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