RecallDepth

Sara Active Sling - Narrow; item KKX053850.0 - models KA1230 (with safety) and KA1240; manufactured by Medibo Medical Products NV, Hanmont, Achel, Belgium, distributed by Arjo Inc., Roselle, IL 60172

Company
Arjo, Inc.
Recall Initiated
January 9, 2007
Posted
February 15, 2007
Terminated
September 2, 2008
Recall Number
Z-0424-2007
Quantity
66 slings
Firm Location
Roselle, IL

Reason for Recall

There is the potential for the slings to come apart, potentially allowing injury to the patient.

Distribution

Nationwide

Lot / Code Info

item KKX053850.0 - models KA1230 (with safety) and KA1240, with production dates of September 2006 through December 2006. The tag on the sling will state the item number and have the year ''06'' hole-punched in the top line ''Y'', and either the month ''09'', ''10'', ''11'' or ''12'' hole-punched in the third line ''M''.

Root Cause

Other

Action Taken

Arjo sent Urgent Device Field Correction Recall Notice letters dated 1/9/07 via FedEx to the end user accounts who received the affected slings, advising them of the potential for the slings to come apart. They were instructed to remove the affected slings from use and replace them with the slings enclosed with the letter, complete the enclosed customer response form, and return the form and the original recalled slings, using the pre-paid call tag provided. If they have any questions or require additional, they were instructed to contact the Arjo Quality Department at 800-323-1245, ext. 6140.

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