PREMIER CARE RECLINER 5570 with Urethane armrests — Class II medical device recall Z-1114-2014
Terminated recall by Winco Mfg., LLC, reported 2014-03-05, distributed nationwide. A supplier manufacturing assembly defect with the right hand recline mechanism. Use of this product may result
| Recall number | Z-1114-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Winco Mfg., LLC, Ocala, FL, United States |
| Recall initiated | 2013-09-06 |
| Classified | 2014-02-26 |
| Reported by FDA | 2014-03-05 |
| Terminated | 2014-12-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, MX |
| Quantity | 369 units |
| Serial numbers | 557A1100178 |
| Model numbers | 5570 |
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.
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1114-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.