# FDA recall Z-0622-2018

> **Medtronic Neurosurgery** · Class II · device recall initiated 2017-12-20.

## Product

Model #: CG8900, Medtronic Clip Gun Scalp Clip Kit (Qty 1); Model #: CG8901, Medtronic Clip Gun Scalp Clip Kit (Qty 10); Model #: CG8901A, Medtronic Clip Gun Applicator (Qty 10)

## Reason for recall

Medtronic is initiating a voluntary recall because the products identified above did not adequately demonstrate acceptable packaging performance to current standards.

## Distribution

Algeria, Armenia, Australia, Canada, Cyprus, Egypt, Germany, Ghana, Greece, Guam, Iceland, Indonesia, Iran, Italy, Jordan, New Zealand, Poland, Portugal, Puerto Rica, Russian Federation, Saudi Arabia, Singapore, South Africa, Spain, Swaziland, Sweden, Switzerland, Syria, Tunisia, Turkey, UAE, UK, USA, Yemen

## Key facts

- **Recall number:** Z-0622-2018
- **Recalling firm:** Medtronic Neurosurgery
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-20
- **Report date:** 2018-02-21
- **Termination date:** 2023-12-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Goleta, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0622-2018

## Citation

> AI Analytics. FDA recall Z-0622-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0622-2018. Source: US FDA. Licensed CC0.

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