# FDA recall Z-2111-2020

> **GE Healthcare, LLC** · Class II · device recall initiated 2020-04-02.

## Product

Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001 GTIN: 00840682110808.

## Reason for recall

During Giraffe Shuttle charging, the batteries emit low concentrations of gases (outgassing) producing a strong sulfur odor.

## Distribution

US Nationwide distribution in the states of AZ, CA, CO, DE, FL, GA, ID, IL, IN, LA, MD, MI, MS, NC, ND, NM, NV, NY, OH, Ok, OR, PA, SC, TN, TX, VA, WA, WI and WV.

## Key facts

- **Recall number:** Z-2111-2020
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-02
- **Report date:** 2020-06-03
- **Termination date:** 2024-05-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2111-2020

## Citation

> AI Analytics. FDA recall Z-2111-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2111-2020. Source: US FDA. Licensed CC0.

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