Winco Mfg., LLC: Medical Device Recall in 2015 - (Recall #: Z-2402-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product 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 Classification:

Class II

Date Initiated: April 2, 2015

Date Posted: August 26, 2015

Recall Number: Z-2402-2015

Event ID: 71496

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.

Status: Terminated

Product Quantity: 29 chairs

Code Information:

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

Distribution Pattern:

Nationwide Distribution including CA, FL, KS, KY, LA, MA, MD, MN, MS, NJ, NY, OK, TN, TX, and WA.

Voluntary or Mandated:

Voluntary: Firm initiated