Giraffe OmniBed¿ and Giraffe Incubator p/n 6600-0723-700 — Class I medical device recall Z-1051-2013
Terminated recall by GE Healthcare, LLC, reported 2013-04-17, distributed in AR, CA, CO, DC, FL, GA, HI, ID…. Neonatal beds and incubator display boards may randomly overwrite stored information and radiant heater and ox
| Recall number | Z-1051-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2013-01-08 |
| Classified | 2013-04-05 |
| Reported by FDA | 2013-04-17 |
| Terminated | 2013-07-10 |
| Distributed | AR, CA, CO, DC, FL, GA, HI, ID, IL, IN, KS, MA, MD, MI, MO, MS, NC, NE, NJ, NV, NY, OH, PA, TN, TX, VA, WA, WI, WV |
| Countries outside the US | AU, BE, BR, CA, CL, CN, CZ, DE, DK, EC, EE, FI, FR, GB, HR, HU, IT, KR, LB, MX, MY, NO, OM, PL, RU, SA, SE, SG, TR, UY, VE, ZA |
| Quantity | 679 units |
| Serial numbers | HDGR52546, HDGR52547, HDGR52558, HDGR52609, HDGR52610, HDGR52613, HDGR52620, HDGR52621, HDGR52622, HDGR52623, HDGR52624, HDGR52626, HDGR52657, HDGR52658, HDGR52664, HDGR52665, HDGR52668, HDGR52669, HDGR52670, HDGR52671, HDGR52672, HDGR52673, HDGR52674, HDGR52675, HDGR52678 and 475 more |
Product
Giraffe OmniBed¿ and Giraffe Incubator p/n 6600-0723-700 (rev A and B) labeled in part: ***GE Healthcare 8880 Gorman Road Laurel, MD 20723 U.S.A. www.gehealthcare.com***. GE Healthcare Giraffe Omnibed is a combination of an infant incubator and an infant warmer.
Reason for recall
Neonatal beds and incubator display boards may randomly overwrite stored information and radiant heater and oxygen set points upon power up or recovery from a power failure.
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-1051-2013. 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.