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

Recall Z-2246-2020 — Centrella Smart+ Bed, Catalog Number P7900

U.S. FDA — Device Enforcement · United States · 2020-04-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2246-2020
Date of alert
2020-04-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Hill-Rom, Inc.
Product category
device
Product type
Devices
Reported risk: The Bed Exit System may fail to send a remote alert through the nurse call system if a remote alert was previously sent and cancelled at the in-room nurse call wall unit.
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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