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

Winco Nocturnal Elite Care Cliner - with Nylon Casters Lay Flat Clinical Patient Recliner w/ Trendelenburg (Long Term Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities) — recall Z-2403-2015

U.S. FDA — Device Enforcement · United States · 2015-04-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2403-2015
Date of alert
2015-04-02
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Winco Mfg., LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
698101503
Reported risk: Shipment of foam for chairs was received classified as Fire Retardant but was in fact standard foam and would not meet Fire Retardant standards.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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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.