PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: June 3, 2020 Initiated: April 2, 2020 #Z-2111-2020

Product Description

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.

Details

Recalling Firm
GE Healthcare, LLC
Units Affected
204 units.
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.
Location
Waukesha, WI

Frequently Asked Questions

What product was recalled?
Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001 GTIN: 00840682110808.. Recalled by GE Healthcare, LLC. Units affected: 204 units..
Why was this product recalled?
During Giraffe Shuttle charging, the batteries emit low concentrations of gases (outgassing) producing a strong sulfur odor.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 3, 2020. Severity: Moderate. Recall number: Z-2111-2020.