SCANLAN International Mobin-Uddin Vein Holder, Sterile, Disposable, single-use, catalog #1001-761, Lot AZ115806.
FDA device recall Z-0701-2007 · posted 2007-04-03 · Terminated
Recall details
- Recalling firm
- Scanlan International Inc
- Reason for recall
- Incorrectly assembled by manufacturer
- Action taken
- 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
- Status
- Terminated
- Product code
- KDC
- Quantity affected
- 35 units domestically ( 70 units to OUS)
- Distribution
- Worldwide distribution --- USA including states of IN, MO and country of Japan
- Date initiated
- 2007-02-19
- Date posted
- 2007-04-03
- Date terminated
- 2007-06-27
- Location
- Saint Paul, MN
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