Giraffe Incubator The Giraffe Incubator is an infant incubator — Class II medical device recall Z-1502-2017
Terminated recall by Ohmeda Medical, reported 2017-03-29, distributed nationwide. Certain power cords could overheat. The affected power cords were manufactured by Electric-Cord and are referr
| Recall number | Z-1502-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ohmeda Medical, Laurel, MD, United States |
| Recall initiated | 2016-11-18 |
| Classified | 2017-03-20 |
| Reported by FDA | 2017-03-29 |
| Terminated | 2018-07-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | BR, BS, CA, CO, CR, EC, ES, GB, HN, IE, JP, LB, MX, NL, PA, SV, TT, TW, VE |
| Reason classes | device malfunction |
Product
Giraffe Incubator The Giraffe Incubator is an infant incubator. Incubators provide heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Incubators provide an enclosed temperature controlled environment
Reason for recall
Certain power cords could overheat. The affected power cords were manufactured by Electric-Cord and are referred to as Taller Bridge power cords. The overheating of the power cord could result in fire, charring, smoke, or sparking where the power cord connects to the wall outlet which could cause thermal injury.
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-1502-2017. 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.