Datex-Ohmeda recalls Giraffe OmniBed Carestation CS1 models with potential incorrect secondary latch on NE/NW bedside panels. Affected units may have safety risk during use.
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 certain Giraffe OmniBed Carestation CS1 models due to a potential incorrect secondary latch on the northeast and northwest bedside panels. This could lead to improper device operation during use, though the risk is not immediately dangerous.
An incorrect secondary latch on the northeast (NE) or northwest (NW) bedside panels could cause the device to become unstable or misaligned during use. This might affect the proper functioning of the carestation, especially in critical infant care settings.
Healthcare facilities using the recalled models, particularly neonatal intensive care units. Parents and caregivers of infants using these devices may be at risk if the latch fails during critical care.
Check for model numbers: a. 2082844-001-XXX, b. 2074920-001-XXXXXX, c. M1050205, d. M1135822, e. M1145475, f. M1145476, g. M1235957, h. M1149051, i. M1146098. Also look for serial numbers listed in the recall notice.
Identify the model number on your device to see if it matches the recalled list: a. 2082844-001-XXX, b. 2074920-001-XXXXXX, c. M1050205, d. M1135822, e. M1145475, f. M1145476, g. M1235957, h. M1149051, i. M1146098.
The recall affects Giraffe OmniBed Carestation CS1 models with specific model numbers: a. 2082844-001-XXX, b. 2074920-001-XXXXXX, c. M1050205, d. M1135822, e. M1145475, f. M1145476, g. M1235957, h. M1149051, i. M1146098.
The recall does not specify a fix or remedy. Affected users should check the model numbers and contact the manufacturer for further guidance.
Check the model number on your device against the list: a. 2082844-001-XXX, b. 2074920-001-XXXXXX, c. M1050205, d. M1135822, e. M1145475, f. M1145476, g. M1235957, h. M1149051, i. M1146098.
We’ve drafted a message you can send Datex-Ohmeda to request your refund or repair — edit it as you like.
Subject: Recall Z-2100-2023 — Datex-Ohmeda Datex-Ohmeda Hello, I own a Datex-Ohmeda that is covered by recall Z-2100-2023 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.
