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# Wipro GE Healthcare Recalls Incubators
- URL: https://www.fdaweb.com/wipro-ge-healthcare-recalls-incubators/
- Published: 2024-02-29T12:00:00.000Z
- Updated: 2026-09-14T14:24:12.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5156457

Wipro GE Healthcare Private Ltd. is recalling (Class 1) its Care Plus and Lullaby Incubators due to the device’s bedside panel or porthole not properly latching closed. “If a bedside panel or porthole is not latched properly, the panel can detach and open, no longer protecting the patient from falling,” a [recall notice](https://www.einpresswire.com/article/692383940/wipro-ge-healthcare-private-ltd-recalls-care-plus-care-plus-models-1000-4000-and-lullaby-incubators-due-to-problems-with-door-latch?ref=fdaweb.com) says. “The use of an affected incubator may lead to falls from the incubator due to improper door closure, and other injuries such as, skin abrasions, bleeding, fractures, and head trauma.” To date, the notice says one report was received of a serious injury from using the device. The incubators are designed to provide heated and humidified air within an enclosed bed compartment for newborns that require body temperature regulation.