The Hospira Plum A+ I.V. Infusion pump is a cassette-based, multi-function fluid delivery infusion system, consisting of
FDA device recall Z-0438-05 · posted 2005-01-27 · Terminated
Recall details
- Recalling firm
- Hospira Inc
- Reason for recall
- The batteries in Plum A+ and Plum A+3 I.V. infusion pumps may fail prematurely when the pump is operating solely on battery power.
- Action taken
- On 9/8/04, all consignees were notified via written letter sent via Federal Express, informing them of the affected products and providing instructions on the recall. The firm will follow up with phone calls to its consignees.
- Root cause
- Other
- Status
- Terminated
- Product code
- JFL
- Quantity affected
- The firm distributed approximately 31,914 units for all model numbers.
- Distribution
- The firm distributed these products to 484 consignees throughout the US, and an undetermined number of foreign consignees. The firm has distributed the product nationwide, excluding AK, HI, NV, NM, SC
- Date initiated
- 2004-09-08
- Date posted
- 2005-01-27
- Date terminated
- 2005-09-20
- Location
- Morgan Hill, CA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| ABBOTT PLUM A+3 MULTICHANNEL INFUSION PUMP, MODEL 12348 (K021350) | Abbott Laboratories | 2002-05-14 |