BD Vacutainer Push Button Blood Collection Set with Pre-Attached holder.
FDA device recall Z-0372-06 · posted 2006-01-11 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- Cracked finger grip luer adapter components on the Push Button Blood Collection Set.
- Action taken
- Recall notification was sent out to the customers on 12/5/2005.
- Root cause
- Other
- Status
- Terminated
- Product code
- KSR
- Quantity affected
- 118200 each
- Distribution
- The device was shipped to 23 wholesalers, 5 hospitals, and 1 VA govt. account nationwide.
- Date initiated
- 2005-12-01
- Date posted
- 2006-01-11
- Date terminated
- 2007-04-30
- Location
- Franklin Lakes, NJ
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| BD VACUTAINER PUSH BUTTON BLOOD COLECTION SET (K011984) | Becton, Dickinson & CO | 2001-08-29 |