PlainRecalls
CPSC Moderate Active

Hair Dryers Recalled for Electrocution Hazard

Reported: July 19, 2006 Initiated: July 19, 2006 #06217

Product Description

The recall involves two models of pistol-type hair dryers: The Monica hair dryer has its model name and number, SW-117, written on the handle. It is made of black plastic and chrome, and the handle folds up. The Turbo 1200 model has model number DS-507 written on the back of the handle. The model name is written on the blower nozzle. They are green and white and green.

Reason for Recall

These electric hair dryers are not equipped with an immersion protection plug to prevent electrocution if the hair dryer falls into water. Such electric shock protection devices are required by industry standards for all electric hand-held hair dryers.

Remedy

Consumers should stop using these hair dryers and contact Style Tronics Inc. for a full refund.

Details

Units Affected
About 19,300
Official Source
https://www.cpsc.gov/Recalls/2006/Hair-Dryers-Recalled-for-Electrocution-Hazard

Frequently Asked Questions

What product was recalled? ▼
The recall involves two models of pistol-type hair dryers: The Monica hair dryer has its model name and number, SW-117, written on the handle. It is made of black plastic and chrome, and the handle folds up. The Turbo 1200 model has model number DS-507 written on the back of the handle. The model name is written on the blower nozzle. They are green and white and green.. Recalled by Style Tronics Inc., of Vernon, Calif.. Units affected: About 19,300.
Why was this product recalled? ▼
These electric hair dryers are not equipped with an immersion protection plug to prevent electrocution if the hair dryer falls into water. Such electric shock protection devices are required by industry standards for all electric hand-held hair dryers.
What should consumers do? ▼
Consumers should stop using these hair dryers and contact Style Tronics Inc. for a full refund.
Which agency issued this recall? ▼
This recall was issued by the CPSC on July 19, 2006. Severity: Moderate. Recall number: 06217.

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 →