Easypump LT 60-24 Easypump Infusion Pump (60 ml x 2 ml/hr)
FDA device recall Z-0741-03 · posted 2003-04-18 · Terminated
Recall details
- Recalling firm
- I-Flow Corporation
- Reason for recall
- Overinfusion due to misassembly.
- Action taken
- Recall letter was sent to sole distributor, B Braun FRance by email on 3/18/2003. Return of stock and subrecall was requested. Consignee has acknowledged implementing subrecall.
- Root cause
- Other
- Status
- Terminated
- Quantity affected
- 2638 units
- Distribution
- Only in France to distributor B. Braun Medical, France
- Date initiated
- 2003-03-18
- Date posted
- 2003-04-18
- Date terminated
- 2003-11-20
- 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 |
|---|---|---|
| HOMEPUMP C-SERIES AND HOMEPUMP C-SERIES ONE-STEP KVO (K991513) | I-Flow Corp. | 1999-06-21 |