FDA Device recall Z-0479-2019

Giraffe OmniBed Carestation

FDA Device
Class II
terminated
Published 2018-11-28

On 2018-11-28 the FDA classified a Class II recall of Giraffe OmniBed Carestation by Ge Healthcare, citing potential electric leakage affecting the user.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0479-2019
Classification	Class II
Status	terminated
Initiated	2018-09-25
Published	2018-11-28
Last updated	2026-09-13 11:54 UTC
Company	Ge Healthcare
Distribution	US

Product

Giraffe OmniBed Carestation. Neonatal incubator. Device sold under the following product names: Carestation and Carestation CS1

Reason

Potential electric leakage affecting the user.

Identifiers

code_info	Model Number, UDI (Serial Number): 2082844-001-526493, 010084068211686221TABX6226911180201 (TABX62269); 2082844-001-5… Model Number, UDI (Serial Number): 2082844-001-526493, 010084068211686221TABX6226911180201 (TABX62269); 2082844-001-526493, 010084068211686221TABX6215911180122 (TABX62159); 2082844-001-526493, 010084068211686221TABX6219811180129 (TABX62198); 2082844-001-526493, 010084068211686221TABX6227011180201 (TABX62270); 2082844-001-526493, 010084068211686221TABX6229111180202 (TABX62291); 2082844-001-526493, 010084068211686221TABX6215611180122 (TABX62156); 2082844-001-526493, 010084068211686221TABX6226011180201 (TABX62260); 2082844-001-526493, 010084068211686221TABX6213511180119 (TABX62135); 2082844-001-526493, 010084068211686221TABX6218911180124 (TABX62189); 2082844-001-526493, 010084068211686221TABX6219611180124 (TABX62196); 2082844-001-526493, 010084068211686221TABX6218811180124 (TABX62188); 2082844-001-526493, 010084068211686221TABX6216011180122 (TABX62160); 2082844-001-487119, To be provided (TABV60550); 2082844-001-526493, 010084068211686221TABW6398711171213 (TABW63987); 20828

code_info

Model Number, UDI (Serial Number): 2082844-001-526493, 010084068211686221TABX6226911180201 (TABX62269); 2082844-001-5…

Model Number, UDI (Serial Number): 2082844-001-526493, 010084068211686221TABX6226911180201 (TABX62269); 2082844-001-526493, 010084068211686221TABX6215911180122 (TABX62159); 2082844-001-526493, 010084068211686221TABX6219811180129 (TABX62198); 2082844-001-526493, 010084068211686221TABX6227011180201 (TABX62270); 2082844-001-526493, 010084068211686221TABX6229111180202 (TABX62291); 2082844-001-526493, 010084068211686221TABX6215611180122 (TABX62156); 2082844-001-526493, 010084068211686221TABX6226011180201 (TABX62260); 2082844-001-526493, 010084068211686221TABX6213511180119 (TABX62135); 2082844-001-526493, 010084068211686221TABX6218911180124 (TABX62189); 2082844-001-526493, 010084068211686221TABX6219611180124 (TABX62196); 2082844-001-526493, 010084068211686221TABX6218811180124 (TABX62188); 2082844-001-526493, 010084068211686221TABX6216011180122 (TABX62160); 2082844-001-487119, To be provided (TABV60550); 2082844-001-526493, 010084068211686221TABW6398711171213 (TABW63987); 20828

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0479-2019%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.