# FDA recall Z-0722-2024

> **Cook Medical Llc** · Class II · device recall initiated 2023-12-07.

## Product

MINC+ Benchtop Incubator, Reference Part Number (RPN) K-MINC-2000, Order Number (GPN) G44429

## Reason for recall

The MINC+ device is susceptible to losing temperature control of electrostatic discharge (static electricity) is applied to the lid of the device. This may lead to embryo degeneration necessitating an additional medical procedure for the patient.

## Distribution

Domestic distribution to CA IN LA MD NY   International distribution to AUSTRALIA AUSTRIA SPAIN FINLAND FRANCE INDIA IRELAND ITALY KUWAIT SWITZERLAND TURKEY UNITED KINGDOM

## Key facts

- **Recall number:** Z-0722-2024
- **Recalling firm:** Cook Medical Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-07
- **Report date:** 2024-01-24

- **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-0722-2024

## Citation

> AI Analytics. FDA recall Z-0722-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0722-2024. Source: US FDA. Licensed CC0.

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