Recalls / —
—#49833
Product
BD Beaver Mini-Blade, Mini/Bulk 67, Catalog Number: 374822
- FDA product code
- HNN — Knife, Ophthalmic
- Device class
- Class 1
- Medical specialty
- Ophthalmic
- Affected lot / code info
- Lot Numbers: 6159386, 6293719
Why it was recalled
Product sterility may be compromised due to incomplete package seal
Root cause (FDA determination)
Other
Action the firm took
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.
Recalling firm
- Firm
- Becton Dickinson and Company
- Address
- 411 Waverley Oaks Rd, Ste 2229, Waltham, Massachusetts 02452-8448
Distribution
- Distribution pattern
- Worldwide, including USA, Asia, Australia, Canada, Mexico, Taiwan, Singapore, Korea, and Japan.
Timeline
- Recall initiated
- 2006-12-26
- Posted by FDA
- 2007-02-08
- Terminated
- 2016-03-07
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #49833. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.