# FDA recall Z-2498-2020

> **CooperSurgical, Inc.** · Class II · device recall initiated 2020-06-03.

## Product

COOPERSURGICAL Os FinderTM Cervical Dilator,   Taper: 2.0 mm to 4.0 mm OD Length: 21.5 cm  Box of 50  Part Number: 1176

## Reason for recall

Mislabeled: Printing on the top web or Tyvek lid  of the individual product blister tray indicating that it contains a Pipet Current or Part Number MX140 and the display box indicating the correct Os FinderTM Cervical Dilators, Part Number 1176. The product in the individual product package is the correct Os Finder Cervical Dilator

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-2498-2020
- **Recalling firm:** CooperSurgical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-03
- **Report date:** 2020-07-15
- **Termination date:** 2021-05-11

- **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-2498-2020

## Citation

> AI Analytics. FDA recall Z-2498-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2498-2020. Source: US FDA. Licensed CC0.

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