Data Foundry

Medical device recalls 2017

Giraffe Exam Light The Exam Light illuminates body surfaces and… — Class II medical device recall Z-1501-2017

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 numberZ-1501-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmOhmeda Medical, Laurel, MD, United States
Recall initiated2016-11-18
Classified2017-03-20
Reported by FDA2017-03-29
Terminated2018-07-13
DistributedNationwide (US)
Countries outside the USBR, BS, CA, CO, CR, EC, ES, GB, HN, IE, JP, LB, MX, NL, PA, SV, TT, TW, VE
Reason classesdevice malfunction

Product

Giraffe Exam Light The Exam Light illuminates body surfaces and facilitates patient observation during a medical examination. It increases ambient light to facilitate performance of procedures on the mattress field. It is designed to mount on the accessory railings of the Giraffe OmniBed, incubators and warmers except for Panda and Giraffe Warmers. It is not intended for use to support surgical field lighting.

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-1501-2017. 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.