Z-1114-2014Class II

PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully...

Name: Z-1114-2014 PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully...
Creator: Winco Mfg., LLC
Published: 2013-09-06
License: https://open.fda.gov/license/

Champion Mfg, Inc. / initiated 2013-09-06 / Terminated / root cause: manufacturing process

FDA source

Winco Mfg., LLC began a recall of PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully upholstered, OPTIONAL Heat or Heat & Massage... on 2013-09-06. FDA classified it as Class II and gives the reason as "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". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-1114-2014
Classification: Class II
Status: Terminated
Initiated: 2013-09-06
Posted: 2014-02-26
Terminated: 2014-12-30
Recalling firm: Champion Mfg, Inc.
Product: PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully upholstered, OPTIONAL Heat or Heat & Massage, OPTIONAL LiquiCell. The products are a multi position recliners with a steel frame used primarily in long term care or convalescent facilities. The recliners are suitable as general purpose seating for relaxation, reclining, eating, patient transport within the facility, and as a patient room chair for visitors.
Product code: INM Chair, With Casters
Reason for recall: 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.
Root cause tag: manufacturing process
FDA root cause: Process control
Action: Winco sent a Recliner Field Correction Notification letter dated September 11, 2013 to all affected consignees. The letter identified the product, the problem and action to be taken by the consignees. The consignees were instructed to complete and return the enclosed field correction response form back to Winco so they can send replacement mechanism(s) along with instructions on how to exchange the mechanism(s). Customers with questions were instructed to contact Customer Care at 800-237-3377 or email [email protected]. For questions regarding this recall call 352-854-2929, ext 130.
Quantity in commerce: 369 units (all models)
Distribution: Worldwide Distribution - USA nationwide including Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Kanas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, New Jersey, New Mexico, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Virginia, Vermont, Washington, Wisconsin, West Virginia, Puerto Rico and Internationally to the country of Canada.
Product codes and lots: Model 5570. Serial numbers: 557A1100178 thru 557A100206.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1114-2014
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1114-2014	Class II	Terminated	Voluntary: Firm initiated	2014-03-05	2014-02-26
Z-1115-2014	Class II	Terminated	Voluntary: Firm initiated	2014-03-05	2014-02-26
Z-1116-2014	Class II	Terminated	Voluntary: Firm initiated	2014-03-05	2014-02-26
Z-1117-2014	Class II	Terminated	Voluntary: Firm initiated	2014-03-05	2014-02-26

Product code INM

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)