# FDA recall Z-2100-2023

> **DATEX--OHMEDA, INC.** · Class II · device recall initiated 2023-05-19.

## Product

Giraffe OmniBed Carestation CS1,   Model Numbers:  a. 2082844-001-XXX,  b. 2074920-001-XXXXXX,  c. M1050205,  d. M1135822,  e. M1145475,  f. M1145476,  g. M1235957,  h. M1149051,  i. M1146098;    Labeled as the following: GIRAFFE OMNIBED CARESTATION CS1, GIRAFFE OMNIBED CARESTATION, GIRAFFE OMNIBED, GIRAFFE OMNIBED CS1, OMNI G 115/230V SERVO2 CARESTATION, ASSY-LAU, OMNIBED CHINA EBASE S HUMID, Manufacturing assembly - Make,  OBSOLETE-Omnibed Czech Servo O2 Nist/Scale/Re-usable Probe/SW w/port hole/CE Plug,  ASSY-LAU, Omnibed Czech S-PH w/Nist O2 w/Reus Probe CE Power Cord, Finished good - Make, ASSY-LAU, Omnibed Czech S-PH w/Reusable Probe CE Power Cord, Finished good - Make, Omnibed Czech Servo O2 Nist/Scale/Re-usable Probe/SW w/port hole/Ce Plug, ASSY-LAU, Omnibed Indonesian S-GR W/Reuseable Probe CE Plug, Finished good - Make, ASSY-LAU, Omnibed ENG S-Gr w/REUProbe CE Power Cord, Finished good - Make, ASSY-LAU, Omnibed Portuguese S-PH w/NIST O2w/Reusable Probe CE Power Cord, Finished

## 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

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-2100-2023
- **Recalling firm:** DATEX--OHMEDA, INC.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-19
- **Report date:** 2023-07-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wauwatosa, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2100-2023

## Citation

> AI Analytics. FDA recall Z-2100-2023. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-2100-2023. Source: US FDA. Licensed CC0.

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