CPSC Recalls

Recalls / 2014-03-18

Schneider Electric Recalls Square D-Brand F and K Frame Circuit Breakers Due to Fire Hazard

14134 · Recalled 2014-03-18 · CPSC page

FA/FH – 1, 2 & 3 Pole
FA/FH – 1, 2 & 3 Pole

Description

This recall involves Square D brand models FA, FH, FI and FY one-, two- and three-pole circuit breakers rated 15 to 100 amps, and model KI two- and three-pole circuit breakers rated 110 to 250 amps. The F model breakers were manufactured May 8, 2013 through June 10, 2013 and have date codes 13193 through 13241. The K models were manufactured May 2, 2013 through June 21, 2013 and have date codes 13184 through 13255. The date codes are YYWWD format (example: 13184 = year 2013, week 18, day of the work week 4/ Thursday). The circuit breakers have a yellow label with the words "Square D" or the Square D logo. Model information can be found on the faceplate.

Hazards

The circuit breaker can fail to trip when an overload occurs, posing the risk of fire, burn and electric shock.

Reported injuries

None reported.

Remedy

Consumers should immediately check to see if they have the recalled circuit breakers. Consumers with uninstalled products will receive a replacement. Installed products will be replaced at no charge to the customer with an allowance of up to $300 per site to cover labor costs.

Products

NameModelUnits
Square D branded, molded case F and K frame circuit breakersAbout 28,400

Parties

Importer
Schneider Electric USA Inc., of Palatine, Ill.
Made in
Mexico
Sold at
Crescent Electric Supply Co., Dealers Electric Supply Co., Graybar Electric Co., Rexel, W.W. Grainger, 260.

Consumer contact

Schneider Electric USA at (800) 634-8730 anytime. Consumers can also visit the firm's website at www.schneider-electric.us and click on "customer notification" under the popular links category for more information.

More images

FI – 2 & 3 Poles and FY – 1 Pole
FI – 2 & 3 Poles and FY – 1 Pole
KI – 2 & 3 Poles I-Line and KI - 2 & 3 Poles
KI – 2 & 3 Poles I-Line and KI - 2 & 3 Poles

Source: CPSC recall 14134. Inclusion in this database is not legal or medical advice.