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

Recall Z-2331-2016 — Spirit Plus Bed, A-C Powered Hospital Bed

U.S. FDA — Device Enforcement · Canada · 2016-06-28 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2331-2016
Date of alert
2016-06-28
Country / jurisdiction
Canada
Risk level
Class II
Risk type
recall
Brand
CHG Hospital Beds Inc
Product category
device
Product type
Devices
Reported risk: Stryker Medical is initiating a voluntary recall of the Spirit Select and Spirit Plus A-C powered hospital beds due to reports of hi-lo actuators broken at the mount ends, which could cause the bed to unexpectedly lower resulting in patient injury.
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.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.