# FDA recall Z-0782-2022

> **Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)** · Class II · device recall initiated 2022-01-18.

## Product

LINQ II Insertable Cardiac Monitor

## Reason for recall

Devices may lose functionality due to susceptibility to moisture ingress.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of NJ, NY, PA, and VA. The country of Italy.

## Key facts

- **Recall number:** Z-0782-2022
- **Recalling firm:** Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-01-18
- **Report date:** 2022-03-23
- **Termination date:** 2026-05-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mounds View, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0782-2022

## Citation

> AI Analytics. FDA recall Z-0782-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0782-2022. Source: US FDA. Licensed CC0.

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