SCANLAN International Mobin-Uddin Vein Holder, Sterile, Disposable, single-use, catalog #1001-761, Lot AZ115806.
FDA Recall Z-0701-2007 · Posted 2007-04-03
Recalling FirmScanlan International Inc
Recall StatusTerminated
Product CodeKDC
Date Initiated2007-02-19
Date Terminated2007-06-27
Product Quantity35 units domestically ( 70 units to OUS)
Reason for Recall
Incorrectly assembled by manufacturer
Firm Action
The consignees were notified of the product recall by letter dated February 19, 2007. Consignees were asked to return product to the manufacturer and replacement product is being offered.
Root Cause
Other
Distribution Pattern
Worldwide distribution --- USA including states of IN, MO and country of Japan
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.