# FDA recall Z-2534-2017

> **Cook Inc.** · Class II · device recall initiated 2017-04-25.

## Product

Pereyra-Raz Ligature Carrier

## Reason for recall

reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and  sterilization of these products

## Distribution

The devices have been distributed nationwide within the United States and the following countries: Australia, Belgium, Canada, Finland, Germany, Guatemala, Hong Kong, India, Ireland, Japan, South Korea, Kuwait, Malaysia, Netherlands, New Zealand, Puerto Rico, Saudi Arabia, Taiwan, and the United Kingdom.

## Key facts

- **Recall number:** Z-2534-2017
- **Recalling firm:** Cook Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-04-25
- **Report date:** 2017-06-21
- **Termination date:** 2019-03-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bloomington, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2534-2017

## Citation

> AI Analytics. FDA recall Z-2534-2017. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-2534-2017. Source: US FDA. Licensed CC0.

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