🔍 RecallPedia

Winco Inverness 24-Hour Treatment Recliner - with Nylon Casters Lay Flat Clinical Patient Recliner w/ Trendelenburg (Long Term Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities)

Class I - Dangerous
🏥 Medical Devices Recalled: April 2, 2015 Winco Mfg. Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Model Number: 6240, Serial Numbers: 624100510, 624100511, 624100512, 624100513, 624100514, 624100515, 624100516, 624100519, 624100520, 624100521, 624100522, 624100523, 624100524, 624100525, 624100526, 624100527, 624100528, 624100529, 624100530, 624100531, 624100532, 624100533, 624100534, 624100535, 624100536, 624100537, 624100538, 624100539 and 624100540
  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 Inverness 24-Hour Treatment Recliner - with Nylon Casters Lay Flat Clinical Patient Recliner w/ Trendelenburg (Long Term Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities)

Product Codes/Lot Numbers:

Model Number: 6240, Serial Numbers: 624100510, 624100511, 624100512, 624100513, 624100514, 624100515, 624100516, 624100519, 624100520, 624100521, 624100522, 624100523, 624100524, 624100525, 624100526, 624100527, 624100528, 624100529, 624100530, 624100531, 624100532, 624100533, 624100534, 624100535, 624100536, 624100537, 624100538, 624100539 and 624100540

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2402-2015

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