# FDA recall Z-1241-2022

> **Cook Incorporated** · Class II · device recall initiated 2022-05-05.

## Product

Nester Embolization Microcoil    RPN                                    GPN    MWCE-18-5-2-NESTER	G52733  MWCE-18-5-3-NESTER	G52734  MWCE-18-7-3-NESTER-01	G47338  MWCE-18-7-2-NESTER-01	G47337  MWCE-18-7-5-NESTER-01	G47340  MWCE-18-3-2-NESTER	G52731  MWCE-18-7-8-NESTER-01	G47342  MWCE-18-7-8-NESTER	G52739  MWCE-18-7-5-NESTER	G23521  MWCE-18-3-3-NESTER	G52732  MWCE-18-5-3-NESTER-01	G47334  MWCE-18-7-6-NESTER	G52738  MWCE-18-7-6-NESTER-01	G47341  MWCE-18-3-3-NESTER-01	G47332  MWCE-18-7-4-NESTER	G52737  MWCE-18-7-3-NESTER	G52736  MWCE-18-3-2-NESTER-01	G47331  MWCE-18-5-2-NESTER-01	G47333  MWCE-18-2-2-NESTER-01	G47344  MWCE-18-5-5-NESTER-01	G47335  MWCE-18-7-2-NESTER	G52735  MWCE-18-7-4-NESTER-01	G47339  MWCE-18-7-10-NESTER	G52741  MWCE-18-5-5-NESTER	G23520

## Reason for recall

The loading cartridges included with these devices may contain a small, unintended, stainless-steel cannula.

## Distribution

Domestic distribution nationwide. Foreign distribution worldwide.

## Key facts

- **Recall number:** Z-1241-2022
- **Recalling firm:** Cook Incorporated
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-05-05
- **Report date:** 2022-06-15

- **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-1241-2022

## Citation

> AI Analytics. FDA recall Z-1241-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1241-2022. Source: US FDA. Licensed CC0.

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