Cozy Comfort Premier Recliner 5580 WITH CAL TB 133 UPGRADE PURCHASED… — Class II medical device recall Z-0779-2013
Terminated recall by Winco Mfg., LLC, reported 2013-02-13, distributed nationwide. The performance of the chemicals in the foam and vinyl are not consistent enough to meet the TB 133 fire prote
| Recall number | Z-0779-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Winco Mfg., LLC, Ocala, FL, United States |
| Recall initiated | 2012-09-24 |
| Classified | 2013-02-04 |
| Reported by FDA | 2013-02-13 |
| Terminated | 2013-05-23 |
| Distributed | Nationwide (US) |
| Quantity | 95 units |
| Serial numbers | 558100022, 558100023, 558100024, 558100025, 558100026, 558A100057, 558A100075 |
| Model numbers | 5580 |
Product
Cozy Comfort Premier Recliner 5580 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012. A multi position recliner with a steel frame used primarily in clinics, hospitals, and treatment centers for recovery, dialysis, oncology, examination, infusion.
Reason for recall
The performance of the chemicals in the foam and vinyl are not consistent enough to meet the TB 133 fire protection mandate required by California and 4 other states.
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-0779-2013. 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.