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

Recall Z-2393-2015 — Winco Care Cliner X-Large - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.

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-2393-2015
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
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.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.

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