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Terminated

BD Beaver Mini-Blade, Blade Mini Pointed Tip S/SU, Catalog Number: 376500

FDA Recall Z-0405-2007 · Posted 2007-02-08

Recalling FirmBecton Dickinson and Company
Recall StatusTerminated
Product CodeHNN
Date Initiated2006-12-26
Date Terminated2016-03-07
Product Quantity47,304 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.

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