KCI USA, Inc. AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA. Power Cord #340225 used with Activac Model 340000, and ActiVAC (Canadian) Model 340013. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA. Power Cord #340225 used with Activac Model 340000, and ActiVAC (Canadian) Model 340013.
Brand
KCI USA, Inc.
Lot Codes / Batch Numbers
Device Serial Numbers: Activac - VDZR00001-VDZR26649, and VCQK00001 - VCQK19781, ActiVAC (Canadian) - VDRK00001 - VDRK00085, VEPR00001 - VEPR01050, and VFSR00150 - VFSR01790.
Products Sold
Device Serial Numbers: Activac - VDZR00001-VDZR26649; and VCQK00001 - VCQK19781; ActiVAC (Canadian) - VDRK00001 - VDRK00085; VEPR00001 - VEPR01050; and VFSR00150 - VFSR01790.
KCI USA, Inc. is recalling AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA. Power Cor due to Power cords may crack and fail inside plug with potential for fire hazard.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Power cords may crack and fail inside plug with potential for fire hazard.
Recommended Action
Per FDA guidance
Kinetics Concepts, Inc. (KCI) issued an "Urgent Medical Device Correction" letter dated November 4, 2009. Consignees were informed of the affected product and instructed to take necessary action to avoid any further issues associated with the product. For further information, contact KCI's technical support team at 1-800-275-4524 option #3.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026