Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

ELITE CARE CLINER 6900 (STD)/6910(X-LG) with Swing-Arm products are labeled in part: "***ELITE CARE CLINER 6900/6910***Winco***ISO 9001-2008 Certified***Design, comfort, durability, and value that exceed your expectations.***Attention to detail and concern for comfort and quality, standards that Winco recliners are known for, places the Elite Care Cliner among the best-selling chairs on the market today. LiquiCell, an ultra-thin liquid filled interface that aids in reducing skin pressure, is standard for the Elite Care Cliner.***HEAT MASSAGE (Optional)***KEY FEATURES***Dual fold down tables***LiquiCell for added comfort***5 nylon total-lock casters***Built-in headrest***Headrest cover***1.800.237.3377***5516 SW 1st Lane***Ocala, Florida 334474***www.wincomfg.com***". Sticker with serial number is labeled in part: "***Manufactured By***Winco***Ocala, FL 34474***www.wincomfg.com*** Model No. ***Serial No.***" The Care Cliner is a multi position recliner with a steel frame used primarily in clinics, hospitals and treatment centers for recovery, dialysis, oncology, examination, infusion.

FDA Recall Z-1459-2012 · Posted 2012-04-25

Recalling FirmWinco Mfg., LLC
Recall StatusTerminated
Product CodeINM
Date Initiated2012-02-06
Date Terminated2012-07-27
Product Quantity613 Casters (189 Chairs)

Reason for Recall

Winco Manufacturing LLC is recalling the Care Cliner, XL Care Cliner, Drop Arm Care Cliner, Elite Care Cliner, and XL Elite Care Cliner chairs with nylon casters distributed between 04/01/2009 and 08/31/2009. Certain 5" nylon casters shipped with the chairs may be defective. There is a potential of the caster's axle working itself out of the assembly under unconventional conditions. Should this

Firm Action

Winco Mfg. sent an "URGENT DEVICE RECALL" letter dated February 1, 2012 to all affected customers. The letter identifies the product, problem, and actions to be taken by the customers. Customers were asked to complete the Caster Recall Replacement Form and return it to the firm's Customer Service Department via fax to 352-854-9544. Contact the Customer Service Department at 800 237-3377 for questions regarding this notice.

Root Cause

Device Design

Distribution Pattern

Worldwide Distribution-USA (nationwide) and the countries of Canada and Singapore.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑