Easypump L T 60-24 infusion pump
FDA device recall Z-0585-06 · posted 2006-03-07 · Terminated
Recall details
- Recalling firm
- I-Flow Corporation
- Reason for recall
- The sterile pack may contain the wrong infusion pump inside.
- Action taken
- The affected customer has been notified with a Notification letter dated January 17, 2006 via e-mail of Recall Notification Letter, with follow-up confirmation e-mails.
- Root cause
- Other
- Status
- Terminated
- Product code
- MEB
- Quantity affected
- 549
- Distribution
- France only
- Date initiated
- 2006-01-17
- Date posted
- 2006-03-07
- Date terminated
- 2007-02-05
- 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 (ON-Q, PAINBUSTER, C-BLOCK, HOMEPUMP, EASYPUMP) (K052117) | I-Flow Corp. | 2005-09-09 |
| HOMEPUMP NSF (K932740) | Block Medical, Inc. | 1993-10-06 |