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Terminated

AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA. Power Cord #4100079 used with Kinair IV Model 22600, Kinair IV 60601 Model 216050, Triadyne Proventa Model 406000, Therapulse ATP/II Models 227800 and 227080.S, Kinair Medsurg Model 201001W, and Kinair Medsurg Pulse Model 40900.

FDA Recall Z-0662-2010 · Posted 2010-01-25

Recalling FirmKCI USA, Inc.
Recall StatusTerminated
Product CodeIOQ
Date Initiated2009-11-04
Date Terminated2011-01-21
Product Quantity4,637 units

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

Official Source

View FDA Recall →

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

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