The Recall Desk
HighFDA (Devices)·Z-2394-2015·Announced 2015-08-26

Winco Care Cliner Chairs Recalled for Non-Fire-Retardant Foam

Winco Mfg. is recalling four Care Cliner X-Large chairs because the foam used was standard foam rather than fire-retardant foam.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a fire hazard in a medical device where the foam does not meet fire retardant standards, but no injuries or illnesses have been reported.

Plain-English summary

Winco Mfg., LLC is recalling four units of the Winco Care Cliner X-Large chair with steel casters. The recall involves Model Number 6541 with serial numbers 654A105210, 654A105204, 654A105208, and 654A105209.

The recall was initiated because the shipment of foam used for the chairs was received classified as fire retardant but was actually standard foam that would not meet fire retardant standards. The chairs were distributed nationwide, including in California, Florida, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Minnesota, Mississippi, New Jersey, New York, Oklahoma, Tennessee, Texas, and Washington.

Consumers should stop using the affected chairs and contact Winco Mfg., LLC for instructions on how to proceed with the recall.

The recalled product

Product
Winco Care Cliner X-Large - with Steel Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
Manufacturer
Winco Mfg., LLC
Hazard
Affected units
4

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 (4)

  • Model Number: 6541
  • Serial Numbers: 654A105210
  • 654A105204
  • 654A105208 and 654A105209.

Distribution

Distributed nationwide across the United States.

The notice also names 15 states specifically:

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.

See all 13 products in this recall →