AC Power Cords, 110V Manufactured by Electri-Cord… recallZ-0665-2010 · KCI USA, Inc. · initiated Nov 4, 2009
Terminated All recalls posted in January 2010
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from KCI USA, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Power cords may crack and fail inside plug with potential for fire hazard.
FDA root cause category: Nonconforming Material/Component
What the company is doing
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.
Recall details
- Recall number
- Z-0665-2010
- Recall class
- Not yet classified by the FDA
- Status
- Terminated
- Initiated by the company
- Nov 4, 2009
- Posted by the FDA
- Jan 25, 2010
- Recalling firm
- KCI USA, Inc.
- Quantity
- 37,437
- Product code
- OMP
- FDA submissions
- K063692
- Distribution
- Nationwide and Canada
Product description
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.
Code information (models, lots, serial numbers)
Device Serial Numbers: Activac - VDZR00001-VDZR26649; and VCQK00001 - VCQK19781; ActiVAC (Canadian) - VDRK00001 - VDRK00085; VEPR00001 - VEPR01050; and VFSR00150 - VFSR01790.
Other devices under the same FDA submission
2 devices cleared under K063692 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
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- ACTIV.A.C.™ M8275058/5 M8275058/10Kci USA, Inc. · Negative Pressure Wound Therapy Powered Suction Pump1 report
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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