# FDA recall Z-1460-2018

> **Cook Inc.** · Class II · device recall initiated 2018-03-22.

## Product

Cook Vacuum Pump (Cook Aspiration Unit) K-MAR-5200-US, GPN G51607.    Intended for the aspiration of body fluids and cells; in particular oocyte aspiration.

## Reason for recall

Pump was found to be constructed from crimp connectors that do not meet the fixation wiring requirements and can cause failure of the device to operate or electric shock or burn to the user.

## Distribution

Worldwide Distribution -- USA, Argentina, Bolivia, Brazil, Canada, Colombia, Guatemala, Mexico, Panama, Peru, Uruguay, and Venezuela.

## Key facts

- **Recall number:** Z-1460-2018
- **Recalling firm:** Cook Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-03-22
- **Report date:** 2018-04-25
- **Termination date:** 2020-05-13

- **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-1460-2018

## Citation

> AI Analytics. FDA recall Z-1460-2018. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1460-2018. Source: US FDA. Licensed CC0.

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