PlainRecalls
CPSC Moderate Active

Berkline Heated Massage Recliners Recalled Due to Burn Hazard; Sold Exclusively at Value City Furniture and American Signature Furniture Stores

Reported: May 11, 2007 Initiated: May 11, 2007 #07547

Product Description

This recall involves the Berkline heated massage recliners with model number 13071 and piece code number 2700. The brand name, the model number, and the piece code can be found on the bill of sale and/or product packaging. The recliners were sold in brown and burgundy.

Reason for Recall

The control device that adjusts the heat and massage settings can overheat, posing a burn hazard to consumers.

Remedy

Consumers should stop using these recliners immediately and contact Value City Furniture or American Signature Furniture to have the recliner removed and to receive a full refund.

Details

Units Affected
About 1,700
Official Source
https://www.cpsc.gov/Recalls/2007/Berkline-Heated-Massage-Recliners-Recalled-Due-to-Burn-Hazard-Sold-Exclusively-at-Value-City-Furniture-and-American-Signature-Furniture-Stores

Frequently Asked Questions

What product was recalled? ▼
This recall involves the Berkline heated massage recliners with model number 13071 and piece code number 2700. The brand name, the model number, and the piece code can be found on the bill of sale and/or product packaging. The recliners were sold in brown and burgundy.. Recalled by Berkline Benchcraft LLC, of Morristown, Tenn.. Units affected: About 1,700.
Why was this product recalled? ▼
The control device that adjusts the heat and massage settings can overheat, posing a burn hazard to consumers.
What should consumers do? ▼
Consumers should stop using these recliners immediately and contact Value City Furniture or American Signature Furniture to have the recliner removed and to receive a full refund.
Which agency issued this recall? ▼
This recall was issued by the CPSC on May 11, 2007. Severity: Moderate. Recall number: 07547.

Related Recalls

FDA Devices Moderate

Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…

Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate

COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…

Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate

Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…

Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate

Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…

Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate

Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…

Fujirebio Diagnostics, Inc. · 2026-02-11

Explore Related Data

Vehicle Safety → Drug Information →