🔍 RecallPedia

PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012. A multi position recliner with a steel frame used primarily in clinics, hospitals, and treatment centers for recovery, dialysis, oncology, examination, infusion.

Class I - Dangerous
🏥 Medical Devices Recalled: September 24, 2012 Winco Mfg. Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Model 5570 and 5574. Serial numbers: 557A100080, 557A100081, 557100004, 557100008, 557100009, 557100012, 557100041, 557100042, 557100043, 557100044, 557100045, 557A100065, 557100036, 557100037, 557100038, 557100039, 557A100073, and 557100048
  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:
The performance of the chemicals in the foam and vinyl are not consistent enough to meet the TB 133 fire protection mandate required by California and 4 other states.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012. A multi position recliner with a steel frame used primarily in clinics, hospitals, and treatment centers for recovery, dialysis, oncology, examination, infusion.

Product Codes/Lot Numbers:

Model 5570 and 5574. Serial numbers: 557A100080, 557A100081, 557100004, 557100008, 557100009, 557100012, 557100041, 557100042, 557100043, 557100044, 557100045, 557A100065, 557100036, 557100037, 557100038, 557100039, 557A100073, and 557100048

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0778-2013

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