# FDA recall Z-2545-2019

> **CooperSurgical, Inc.** · Class III · device recall initiated 2019-08-19.

## Product

LEEP Return Patient Pads (10/ box)  Model # 6050Pl   used in electrosurgical procedures.

## Reason for recall

Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect expiration dates on the outer boxes, where the month and day were reversed.

## Distribution

USA: AK, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME,  MI, MN, MO, MS, NC, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, & WV.    Distribution US nationwide, Canada, Colombia, Japan, & Malaysia

## Key facts

- **Recall number:** Z-2545-2019
- **Recalling firm:** CooperSurgical, Inc.
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-08-19
- **Report date:** 2019-09-25
- **Termination date:** 2020-07-14

- **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-2545-2019

## Citation

> AI Analytics. FDA recall Z-2545-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2545-2019. Source: US FDA. Licensed CC0.

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