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

Recall Z-1115-2014 — CONVALESCENT RECLINER 5251/5261, 525S/526S with Side Storage Pocket, Upholstered side-panels, Recessed hand-grips, Webbed suspension seating, Non-porous tray. The products are a multi position recliners with a steel frame used primarily in long term care or convalescent facilities. The recliners

U.S. FDA — Device Enforcement · United States · 2013-09-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1115-2014
Date of alert
2013-09-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Winco Mfg., LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
525108626
Reported risk: A supplier manufacturing assembly defect with the right hand recline mechanism. Use of this product may result in the loss of functionality of the three (3) position lock bar when in a reclined position.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.