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

Recall Z-1864-2012 — Advanta 2 Bed. The Advanta 2 Bed is intended for low to moderate acuity patients in the medical/surgical area of the hospital.

U.S. FDA — Device Enforcement · United States · 2012-06-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1864-2012
Date of alert
2012-06-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Hill-Rom, Inc.
Product category
device
Product type
Devices
Reported risk: During an evaluation of Advanta 2 siderail samples returned from the field it was found that the screws used to attach the siderail were being stripped from the plastic cavity of the siderail.
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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