Beside panel FRU — Class II medical device recall Z-2102-2023
Ongoing recall by DATEX--OHMEDA, INC., reported 2023-07-12. GE HealthCare has become aware of the potential that an incorrect type of secondary latch could have been inst
| Recall number | Z-2102-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | DATEX--OHMEDA, INC., Wauwatosa, WI, United States |
| Recall initiated | 2023-05-19 |
| Classified | 2023-07-06 |
| Reported by FDA | 2023-07-12 |
| Quantity | 18 |
| Model numbers | 5865384-01, 5865384-34, 5865385-01, 5865385-34, 5865386-01, 5865386-34, 5865387-01, 5865387-34 |
Product
Beside panel FRU (Field Replacement Units) Kits
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2102-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.