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.
What this means for you
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
- Hazard
- 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
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 →Related recalls
Same manufacturer · Winco Mfg., LLC
See all →- ModerateWinco TMM5 Mobile Surgical Stretcher-Chair Recalled for Design Non-Conformance
FDA (Devices) · 2016-10-19
- ModerateWinco TMM4 Series Treatment Chair Recalled for Non-Conforming Component
FDA (Devices) · 2016-10-19
- ModerateWinco TMM3 Video-Fluoroscopy Stretcher-Chair Recalled for Non-Conforming Component
FDA (Devices) · 2016-10-19
- HighWinco Drop Arm Care Cliner Chairs Recalled for Fire Hazard
FDA (Devices) · 2015-08-26
- SevereWinco Designer Care Cliner Recalled for Non-Fire Retardant Foam
FDA (Devices) · 2015-08-26
Same hazard · fire
See all →- HighKibbi Recalls 2026-2027 Renegade RVs Due to Fire Risk
NHTSA · 2026-09-05
- SevereAmana Through-The-Wall Air Conditioners Recalled Due to Fire Risk
CPSC · 2026-09-03
- Severe
- High
- SevereTiffin Recalls 2026-2027 Wayfarer RVs Due to LP Tank Defects
NHTSA · 2026-08-31