# FDA recall Z-0624-2018

> **Aesculap Implant Systems LLC** · Class II · device recall initiated 2017-09-08.

## Product

JS Series SterilContainer S2 System

## Reason for recall

The JS Series SterilContainer S2 System was released to the market place prior to an authorized FDA 510K clearance. No other Aesculap SterilContainer System products are impacted by this recall.

## Distribution

Nationally

## Key facts

- **Recall number:** Z-0624-2018
- **Recalling firm:** Aesculap Implant Systems LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-08
- **Report date:** 2018-02-21
- **Termination date:** 2019-04-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Center Valley, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0624-2018

## Citation

> AI Analytics. FDA recall Z-0624-2018. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-0624-2018. Source: US FDA. Licensed CC0.

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