Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0540-2020 — Giraffe Incubator Carestation, Giraffe Incubator Carestation CS1 infant warmer

U.S. FDA — Device Enforcement · United States · 2019-10-11 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0540-2020
Date of alert
2019-10-11
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
GE Healthcare, LLC
Product category
device
Product type
Devices
Reported risk: Giraffe Incubator, Giraffe OmniBed, Giraffe Incubator Carestation, and Giraffe OmniBed Carestation Bedside panels and portholes can appear closed without being latched. Potential patient fall.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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