Winco Mfg., LLC: Medical Device Recall in 2013 - (Recall #: Z-0777-2013)

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 LIFECARE RECLINER 5400 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-0777-2013

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 5400. Serial numbers: 540100017, 540100020, 540100063, 540100160, 540100161, 540100162, 540100062, 540100103, 540100104, 540100105, and 540100106.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated