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Terminated

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.

FDA Recall Z-0665-2010 · Posted 2010-01-25

Recalling FirmKCI USA, Inc.
Recall StatusTerminated
Product CodeOMP
Date Initiated2009-11-04
Date Terminated2011-01-21
Product Quantity37,437

Reason for Recall

Power cords may crack and fail inside plug with potential for fire hazard.

Firm Action

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.

Root Cause

Nonconforming Material/Component

Distribution Pattern

Nationwide and Canada

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K063692V.A.C. THERAPY SYSTEMS-ACTI V.A.C. THERAPY UNIT MODEL# 340000Kci USA, Inc. · 2007-06-07

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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