Datex-Ohmeda recalls Beside panel FRU kits for certain Giraffe OmniBed devices due to potential incorrect secondary latch installation, which could cause panel detachment. Affected kits include models 5865384-01 to 5865384-34, 5865385-01 to 5865385-34, 5865386-01 to 5865386-34, and 5865387-01 to 5865387-34.
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
Datex-Ohmeda is recalling Beside panel FRU kits for certain Giraffe OmniBed devices because an incorrect secondary latch might be installed, potentially causing the panel to detach. This could lead to injury if the panel becomes loose during use.
An incorrect secondary latch could be installed on the northeast or northwest bedside panels. If the panel becomes loose, it might detach from the device, posing a risk of injury to patients or staff during use.
Healthcare facilities using the affected Beside panel FRU kits for Giraffe OmniBed devices are most at risk. Patients or staff could be injured if the panel detaches during use.
Check if your kit has model numbers 5865384-01 to 5865384-34, 5865385-01 to 5865385-34, 5865386-01 to 5865386-34, or 5865387-01 to 5865387-34. These kits are for Giraffe OmniBed and Giraffe OmniBed Carestation devices.
Identify if your kit has model numbers 5865384-01 to 5865384-34, 5865385-01 to 5865385-34, 5865386-01 to 5865386-34, or 5865387-01 to 5865387-34.
An incorrect secondary latch could be installed, potentially causing the panel to detach during use, which might lead to injury.
Check the model numbers on the kit: 5865384-01 to 5865384-34, 5865385-01 to 5865385-34, 5865386-01 to 5865386-34, or 5865387-01 to 5865387-34.
No, but you should check if your kit is affected and take action if it is.
We’ve drafted a message you can send Datex-Ohmeda to request your refund or repair — edit it as you like.
Subject: Recall Z-2102-2023 — Datex-Ohmeda Datex-Ohmeda Hello, I own a Datex-Ohmeda that is covered by recall Z-2102-2023 from Datex-Ohmeda. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
