Agency classClass IIOur severity:High FDA (Devices)·Z-2402-2015·Announced 2015-08-26

Winco Inverness Recliners Recalled for Fire Retardant Foam Mislabeling

Winco Mfg. is recalling 29 Inverness recliners because the foam was mislabeled as fire retardant but is actually standard foam.

The agency’s classification

FDA (Devices): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 3/5 (High).

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a risk-of-harm product (fire hazard) where injury has not yet been reported, fitting the criteria for a High severity score.

Plain-English summary

Winco Mfg., LLC is recalling 29 units of the Winco Inverness 24-Hour Treatment Recliner, Model Number 6240. The recall involves specific serial numbers ranging from 624100510 to 624100540, with some numbers in that sequence excluded. These chairs were distributed nationwide, including in California, Florida, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Minnesota, Mississippi, New Jersey, New York, Oklahoma, Tennessee, Texas, and Washington.

The recall was initiated because a shipment of foam intended for these chairs was received classified as fire retardant but was actually standard foam that does not meet fire retardant standards. This misclassification means the product does not provide the fire safety characteristics indicated by its labeling.

Consumers who possess these specific recliners should stop using them and contact Winco Mfg., LLC for further instructions on the recall process.

The recalled product

Product: 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)
Manufacturer: Winco Mfg., LLC
Category: Medical Device — Patient Recliner
Hazard: fire
mis-labeling
Affected units: 29

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

Model Number: 6240
Serial Numbers: 624100510
624100511
624100512
624100513
624100514
624100515
624100516
624100519
624100520
624100521
624100522
624100523
624100524
624100525
624100526
624100527
624100528
624100529
624100530

Distribution

Distributed nationwide across the United States.

The notice also names 15 states specifically:

Part of a larger recall action

This product is one of 13 recalled by Winco Mfg., LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 13 products in this recall →

Same manufacturer · Winco Mfg., LLC

See all →

Moderate
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FDA (Devices) · 2016-10-19
Moderate
Winco TMM4 Series Treatment Chair Recalled for Non-Conforming Component
FDA (Devices) · 2016-10-19
Moderate
Winco TMM3 Video-Fluoroscopy Stretcher-Chair Recalled for Non-Conforming Component
FDA (Devices) · 2016-10-19
High
Winco Drop Arm Care Cliner Chairs Recalled for Fire Hazard
FDA (Devices) · 2015-08-26
Severe
Winco Designer Care Cliner Recalled for Non-Fire Retardant Foam
FDA (Devices) · 2015-08-26

Same hazard · fire