FDA Recall Terminated

MTD 4000 - Mettler Traction Decompression System, Model: ME 4000 Product Usage: Provide traction and mobilization of skeletal structures and skeletal muscles

Recall: Z-2580-2011 · Initiated April 14, 2011

Recall

Recall Number
Z-2580-2011
Event Number
58787
Firm
Mettler Electronics Corp
FEI Number
2013558
Product Code
ITH
Status
Terminated
Root Cause
Device Design
Initiated
April 14, 2011
Posted
June 17, 2011
Terminated
July 10, 2012
Address
1333 S Claudina St, Anaheim, CA, 92805

Description

MTD 4000 - Mettler Traction Decompression System, Model: ME 4000 Product Usage: Provide traction and mobilization of skeletal structures and skeletal muscles

Reason

The recall was initiated because Mettler has confirmed the possible failure of internal mechanical component and software detection for potential failure regarding Electronics Traction Device - MTD4000. The firm are initiating the recall because component failure might result in patient injury. Use of the device should cease immediately.

Action

Mettler Electronics sent an "URGENT MEDICAL DEVICE RECALL" letter dated April 14, 2011 to all affected consignees. The letter identified the product, the problem and the actions to be taken. Customers were instructed to immediately cease use of the recalled device, examine their inventory and quarantine product subject to recall. In addition, consignees were told if they have further distributed the affected product to please identify their customers and notify them at once of this product recall. The letter asks that that each includes a "Recall Return Response Form" that consignees are required to complete and return. If you have any questions please contact Mettler Electronics Corp 714-533-2221 x331, Monday through Friday, between the hours of 8:30 A.M. and 4:00 P.M. Pacific Time.

Distribution

Worldwide Distribution --USA (nationwide) and countries of Taiwan, Ireland and Haiti.

Quantity

221