KCI USA, Inc. AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA. Power Cord #M4268840 used with First Step All-In-One Canadian French Models 227500-09 and 227500, First Step All-In-One English Model 227500, Therakair Visio Models M8259978 and M6257763 pump only, and Proficare - Canada Model M8259988 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 #M4268840 used with First Step All-In-One Canadian French Models 227500-09 and 227500, First Step All-In-One English Model 227500, Therakair Visio Models M8259978 and M6257763 pump only, and Proficare - Canada Model M8259988
Brand
KCI USA, Inc.
Lot Codes / Batch Numbers
Device Serial Numbers: First Step All-In-One 35 Inch Canadian French - FTGK00001-FTGK00106, First Step All-In One 35-Inch English - FTCK00001-FTCK00624, Therakair Visio Canadian 800 Wids, Therakair Visio Canadian 900 Wids, Airworks Sure Std. 110V-Canada, Airworks Sure 80CM Wide, 110V - Canada, Product Assy-Provicare Std. 110V-Canada, and Product Assy-Proficare 80CM wide, 110V-Canada.
Products Sold
Device Serial Numbers: First Step All-In-One 35 Inch Canadian French - FTGK00001-FTGK00106; First Step All-In One 35-Inch English - FTCK00001-FTCK00624; Therakair Visio Canadian 800 Wids; Therakair Visio Canadian 900 Wids; Airworks Sure Std. 110V-Canada; Airworks Sure 80CM Wide, 110V - Canada; Product Assy-Provicare Std. 110V-Canada; and Product Assy-Proficare 80CM wide, 110V-Canada.
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