Winco Drop Arm Care Cliner Standard — Class II medical device recall Z-2395-2015
Terminated recall by Winco Mfg., LLC, reported 2015-08-26, distributed nationwide. Shipment of foam for chairs was received classified as Fire Retardant but was in fact standard foam and would
| Recall number | Z-2395-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Winco Mfg., LLC, Ocala, FL, United States |
| Recall initiated | 2015-04-02 |
| Classified | 2015-08-14 |
| Reported by FDA | 2015-08-26 |
| Terminated | 2016-12-14 |
| Distributed | Nationwide (US) |
| Quantity | 30 chairs |
| Serial numbers | 655A108119, 655A108120, 655A108121, 655A108122, 655A108123, 655A108124, 655A108125, 655A108126, 655A108127, 655A108128, 655A108129, 655A108130, 655A108131, 655A108132, 655A108133, 655A108134, 655A108135, 655A108136, 655A108137, 655A108138, 655A108139, 655A108140, 655A108141, 655A108142, 655A108143 and 5 more |
| Model numbers | 6550 |
Product
Winco Drop Arm Care Cliner Standard - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
Reason for recall
Shipment of foam for chairs was received classified as Fire Retardant but was in fact standard foam and would not meet Fire Retardant standards.
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-2395-2015. 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.