Recall Z-2391-2015— Winco Mfg., LLC
Class II · Terminated
Class II FDA medical device recall by Winco Mfg., LLC, initiated 2015-04-02, terminated 2016-12-14. FDA's recall record names no specific 510(k) clearance for this event. Product: Winco XL Convalescent Recliner - with Steel Casters Long term patient recliner (Nursing, Rehabilitation, Geriatric Home Use, Retirement facilities). Reason: Shipment of foam for chairs was received classified as Fire Retardant but was in fact standard foam and would not meet Fire Retardant standards..
- Recalling firm
- Winco Mfg., LLC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-04-02
- Terminated
- 2016-12-14
- Firm location
- Ocala, FL, United States
Product description
Winco XL Convalescent Recliner - with Steel Casters Long term patient recliner (Nursing, Rehabilitation, Geriatric Home Use, Retirement 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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.