Z-0407-2007

BD Beaver Mini-Blade, Blade Mini Sharp All Around S/SU, Catalog Number: 376900

Name: Z-0407-2007 BD Beaver Mini-Blade, Blade Mini Sharp All Around S/SU, Catalog Number: 376900
Creator: Becton Dickinson and Company
Published: 2006-12-26
License: https://open.fda.gov/license/

Becton Dickinson & Co / initiated 2006-12-26 / Terminated / root cause: packaging

FDA source

Becton Dickinson and Company began a recall of BD Beaver Mini-Blade, Blade Mini Sharp All Around S/SU, Catalog Number: 376900 on 2006-12-26. The reason FDA records is "Product sterility may be compromised due to incomplete package seal". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-0407-2007
Status: Terminated
Initiated: 2006-12-26
Posted: 2007-02-08
Terminated: 2016-03-07
Recalling firm: Becton Dickinson & Co
Product: BD Beaver Mini-Blade, Blade Mini Sharp All Around S/SU, Catalog Number: 376900
Product code: HNN Knife, Ophthalmic
Reason for recall: Product sterility may be compromised due to incomplete package seal
Root cause tag: packaging
FDA 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 in commerce: 136,032 units
Distribution: Worldwide, including USA, Asia, Australia, Canada, Mexico, Taiwan, Singapore, Korea, and Japan.
Product codes and lots: Lot Numbers: 6137932, 6142435, 6158382, 6180374, 6187250, 6192282, 6194468, 6198656, 6209256, 6220182, 6223296, 6234908, 6240871, 6243911, 6248083, 6261021, 6271650, 6276887 6283485* 6289455* 6304844* 6317038* 6333608* 6338256* 6342185*

Product code HNN

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)