# FDA recall Z-2405-2021

> **Clarus Medical, Llc** · Class II · device recall initiated 2021-07-27.

## Product

Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002

## Reason for recall

The sterile barrier seal may be compromised.

## Distribution

Distribution in US - 18 accounts 1 foreign account

## Key facts

- **Recall number:** Z-2405-2021
- **Recalling firm:** Clarus Medical, Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-07-27
- **Report date:** 2021-09-08
- **Termination date:** 2022-09-15

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2405-2021

## Citation

> AI Analytics. FDA recall Z-2405-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2405-2021. Source: US FDA. Licensed CC0.

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