BD Beaver Mini-Blade, Blade Mini Sharp All Around S/SU, Catalog Number: 376900
FDA Recall Z-0407-2007 · Posted 2007-02-08
Recalling FirmBecton Dickinson and Company
Recall StatusTerminated
Product CodeHNN
Date Initiated2006-12-26
Date Terminated2016-03-07
Product Quantity136,032 units
Reason for Recall
Product sterility may be compromised due to incomplete package seal
Firm Action
On 12/26/2006 BD Medical, Ophthalmic Systems mailed a recall notification letter to US Distributors and US OEM''s. Customers are instructed to return any affected products to BD for a replacement.
On 1/10/07, the firm expanded the recall to additional lots. Those lots are noted with an asterisk.
Root Cause
Other
Distribution Pattern
Worldwide, including USA, Asia, Australia, Canada, Mexico, Taiwan, Singapore, Korea, and Japan.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.