ProLong Continuous Nerve Block Set model nubers PL-50 and PL-100
FDA device recall Z-1003-03 · posted 2003-07-15 · Terminated
Recall details
- Recalling firm
- Life-Tech International, Inc
- Reason for recall
- Catheter does not fit through the needle resulting in delay of medical procedure
- Action taken
- The firm initiated the recall via letter to all consignees on May 9, 2001.
- Root cause
- Other
- Status
- Terminated
- Product code
- CAZ
- Distribution
- CA, MN, TX, FL, UT,
- Date initiated
- 2001-05-09
- Date posted
- 2003-07-15
- Date terminated
- 2003-07-15
- Location
- Stafford, TX
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| PROLONG, MODELS PL50, PL100, PL150 (K001129) | Life-Tech Intl., Inc. | 2000-07-06 |