DATEX--OHMEDA, INC.: Medical Device Recall in 2023 - (Recall #: Z-2102-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Beside panel FRU (Field Replacement Units) Kits

Product Classification:

Class II

Date Initiated: May 19, 2023

Date Posted: July 12, 2023

Recall Number: Z-2102-2023

Event ID: 92454

Reason for Recall:

GE HealthCare has become aware of the potential that an incorrect type of secondary latch could have been installed on the northeast (NE) and/or northwest (NW) bedside panels for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices

Status: Ongoing

Product Quantity: 18

Code Information:

Models: 5865384-01 to 5865384-34, 5865385-01 to 5865385-34, 5865386-01 to 5865386-34 and 5865387-01 to 5865387-34

Distribution Pattern:

Worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated