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

Recall Z-0228-2025 — a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed, Product codes: P7900B000001, P7900B100010, P7900B100024, P7900B100208, P7900B100273, P7900B100304, P7900B000005, P7900B100011, P7900B100025, P7900B100212, P7900B100277, P7900B100307, P7900B000010, P7900B100017, P7900B100026, P7900B100222,

U.S. FDA — Device Enforcement · United States · 2024-09-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0228-2025
Date of alert
2024-09-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00887761985162
Reported risk: The beds have a potential for an interface issue with the Rauland Responder 5 Nurse Call System where the bed exit system will alert at the bed, but may fail to send a remote alert through the nurse call system.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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