Winco Designer Care Cliner Recalled for Non-Fire Retardant Foam
Winco Mfg. is recalling Designer Care Cliner chairs because the foam used was not fire retardant as required.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall involves a fire safety defect where the product fails to meet fire retardant standards, posing a significant fire hazard risk.
Plain-English summary
Winco Mfg., LLC is recalling one unit of the Winco Designer Care Cliner w/Swing Arms - with Nylon Casters (Model Number 6740). The recall is due to a material defect where the foam used in the chair was received as standard foam rather than the required fire retardant foam. Consequently, the product does not meet fire retardant standards.
The affected chair is intended for use in oncology, dialysis, hospital recovery, home dialysis, and physician facilities. The product was distributed nationwide, including in California, Florida, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Minnesota, Mississippi, New Jersey, New York, Oklahoma, Tennessee, Texas, and Washington.
Consumers and facilities should stop using the affected chair immediately. Winco Mfg., LLC is the recalling firm responsible for the recall.
The recalled product
- Product
- Winco Designer Care Cliner w/Swing Arms - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
- Manufacturer
- Winco Mfg., LLC
- Hazard
- Affected units
- 1
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Model Number: 6740
Distribution
Part of a larger recall action
This product is one of 13 recalled by Winco Mfg., LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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