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

Recall Z-0031-2013 — Caremor Cliner"Manufactured By WincoOcala, FL 34474 www.wincomfg.comModel No. 536 Serial No. 536A-101475" Literature: "Caremor Cliner 5351/5361WincoISO 9001-2008 CertifiedOur most comfortable and versatile recliner***Ease of operation, outstanding durability, and exceptio

U.S. FDA — Device Enforcement · United States · 2012-07-10 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0031-2013
Date of alert: 2012-07-10
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Winco Mfg., LLC
Product category: device
Product type: Devices

Reported risk: Winco Mfg., LLC in Ocala, FL is recalling the Caremor Cliner model numbers 5351 and 5361. The recall was initiated due to a report that a back frame did not "snap" onto a chair frame properly.

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.

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