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

Recall Z-2082-2012 — Affinity Four Birthing Bed P3700 Product Usage: The Affinity, Four Birthing Bed is intended to be used as birthing beds for women of child bearing age in an LDR (Labor, Delivery, Recovery ) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market.

U.S. FDA — Device Enforcement · United States · 2012-04-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2082-2012
Date of alert
2012-04-02
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Hill-Rom, Inc.
Product category
device
Product type
Devices
Reported risk: During review of our last braking system via that field corrective action, the system still did not meet our expectations, which is to eliminate the hazards of patient falling. Bed movement immediately prior to, or during the birthing process may still create distractions and delays, resulting in patient or caregiver falls, or contribute to a deviation in a procedure, (e.g. IV insertion, epidural
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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