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

Recall Z-0942-2017 — TRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen 1). Mobility Medical Device

U.S. FDA — Device Enforcement · United States · 2016-12-01 · 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-0942-2017
Date of alert
2016-12-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Pride Mobility Products Corp
Product category
device
Product type
Devices
Reported risk: The interface between the TB3 back and tilt base can separate when tilted beyond the specified angle.
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.

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.