Scanlan International Inc SCANLAN International Mobin-Uddin Vein Holder, Sterile, Disposable, single-use, catalog #1001-761, Lot AZ115806. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SCANLAN International Mobin-Uddin Vein Holder, Sterile, Disposable, single-use, catalog #1001-761, Lot AZ115806.
Brand
Scanlan International Inc
Lot Codes / Batch Numbers
Lot AZ115806.
Products Sold
Lot AZ115806.
Scanlan International Inc is recalling SCANLAN International Mobin-Uddin Vein Holder, Sterile, Disposable, single-use, catalog #1001-761, L due to Incorrectly assembled by manufacturer. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrectly assembled by manufacturer
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN, MO
Page updated: Jan 10, 2026