FDA Medical Device Recalls (openFDA)
Becton Dickinson and Company: BD Beaver Mini-Blade, Mini/Bulk 69, Catalog Number: 374823
- Recall number
- Z-0410-2007
- Recalling firm
- Becton Dickinson and Company
- Product
- BD Beaver Mini-Blade, Mini/Bulk 69, Catalog Number: 374823
- Status
- Terminated
- Initiated
- 2006-12-26
- Posted
- 2007-02-08
- Terminated
- 2016-03-07
- Reason
- Product sterility may be compromised due to incomplete package seal
- Root cause
- Other
- 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.
- Quantity
- 43,600 units
- Distribution
- Worldwide, including USA, Asia, Australia, Canada, Mexico, Taiwan, Singapore, Korea, and Japan.
- Lot, serial or model codes
- Lot Numbers: 6151098, 6202027, 6216915, 6227071, 6237675, 6276883 6293717*
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- HNN
- Firm FEI
- 1211998
- Firm city
- Waltham
- Firm state
- MA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28