Eclipse Infusion Pump, 250 ml X 250 ml per hour) Part 5001247
FDA device recall Z-0312-04 · posted 2004-01-09 · Terminated
Recall details
- Recalling firm
- I-Flow Corporation
- Reason for recall
- Slower than expected infusion of medications, such as antibiotics.
- Action taken
- All customers were contacted by telephone on 8/19/2002. Letters were also sent dated 8/27/2002. Recall is complete.
- Root cause
- Other
- Status
- Terminated
- Product code
- MEB
- Quantity affected
- 144
- Date initiated
- 2002-08-19
- Date posted
- 2004-01-09
- Date terminated
- 2005-01-04
- Location
- Lake Forest, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| I-FLOW ELASTOMERIC PUMP (K020862) | I-Flow Corp. | 2002-03-26 |