Winco Mfg., LLC: Medical Device Recall in 2013 - (Recall #: Z-0778-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product 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 Classification:

Class II

Date Initiated: September 24, 2012

Date Posted: February 13, 2013

Recall Number: Z-0778-2013

Event ID: 63651

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.

Status: Terminated

Product Quantity: 95 units (All models)

Code Information:

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

Distribution Pattern:

Nationwide Distribution including CA, FL, IL, MA, MD, MN, NM, NY, OH, OK, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated