Winco Elite Care Cliner w/Swing Away Arms X-Large - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Model Number: 6950, Serial Numbers: 695104466, 695104467, 695104445, 695104273, 695104460, 695104461, 695104462, 695104463, 695104464, 695104465, 695104450, 695104451, 695104452, 695104431, 695104438, 695104442, 695104444, 695104437, 695104438, 695104439, 695104440, 695104441, 695104442, 695104443, 695104444, 695104439 and 695104437 694A106091, 694A106092, 694A106093, 694A106094, 694A106095, 694A106096, 694A106097, 694A106098, 694A106099, 694A106034, 694A106035, 694A106036, 694A106037, 694A106038, 694A106039, 694A106040, 694A106041, 694A106042, 694A106043, 694A106044, 694A106045, 694A106087, 694A106088, 694A106089, 694A106058 and 694A106099
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Winco Mfg., LLC
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Winco Elite Care Cliner w/Swing Away Arms X-Large - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.

Product Codes/Lot Numbers:

Model Number: 6950, Serial Numbers: 695104466, 695104467, 695104445, 695104273, 695104460, 695104461, 695104462, 695104463, 695104464, 695104465, 695104450, 695104451, 695104452, 695104431, 695104438, 695104442, 695104444, 695104437, 695104438, 695104439, 695104440, 695104441, 695104442, 695104443, 695104444, 695104439 and 695104437 694A106091, 694A106092, 694A106093, 694A106094, 694A106095, 694A106096, 694A106097, 694A106098, 694A106099, 694A106034, 694A106035, 694A106036, 694A106037, 694A106038, 694A106039, 694A106040, 694A106041, 694A106042, 694A106043, 694A106044, 694A106045, 694A106087, 694A106088, 694A106089, 694A106058 and 694A106099

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2401-2015

Related Recalls