BD L-Cath NN (24ga x 30cm), L-Cath Catheter System
FDA device recall Z-0783-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Becton Dickinson Infusion Therapy
- Reason for recall
- Catheters have stylets extending past the catheter tip, which, if not noticed could cause injury upon insertion.
- Action taken
- All consignees were notified by telephone on 03/09/2004, followed by a fax letter.
- Root cause
- Other
- Status
- Terminated
- Product code
- LJS
- Quantity affected
- 5690 units
- Distribution
- Nationwide. Foreign distribution to Australia, Canada and Japan.
- Date initiated
- 2004-03-09
- Date posted
- 2004-07-20
- Date terminated
- 2011-06-24
- Location
- Sandy, UT
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| L-CATH PEEL AWAY SYSTEM CATHETER (K920755) | Luther Medical Products, Inc. | 1993-06-07 |