CE INFUSOR LV10, 12 PACK
Report
- Report Number
- 6000001-2010-01751
- Event Type
- Malfunction
- Date Received
- July 19, 2010
- Date of Event
- June 30, 2010
- Report Date
- July 1, 2010
- Manufacturer
- BAXTER HEALTHCARE - IRVINE
- Product Code
- MEB
- PMA / PMN Number
- K071222
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AS
- Reporter Occupation
- OTHER
Narratives
(B)(4). THE CUSTOMER DID NOT SEND THE DEVICE TO BAXTER FOR EVALUATION. THEREFORE, THE REPORTED CONDITION OF THE DEVICE DELIVERING FASTER THAN INTENDED COULD NOT BE CONFIRMED. SHOULD THE SAMPLE AND/OR ADDITIONAL INFORMATION BE RECEIVED, A FOLLOW-UP MEDWATCH WILL BE SUBMITTED.
(B)(4). ADDITIONAL INFORMATION:A BATCH REVIEW WAS PERFORMED FINDING THAT NO EXCEPTION/NON-CONFORMANCE REPORTS WERE DOCUMENTED FOR THIS LOT. ALL RELEASE CRITERIA WERE MET FOR THE BUILD OF THE LOT.
PER THE CLINIC, THE PATIENT EXPERIENCED A PERFORMANCE DECREMENT, RESULTING IN THE DECISION TO EXPLANT THE DEVICE. THE DEVICE WAS EXPLANTED (B)(6), 2009, AND THE PATIENT WAS REIMPLANTED WITH A NEW DEVICE DURING THE SAME SURGERY.
IT WAS REPORTED TO BAXTER (B)(4) THAT AN INFUSOR LV 10 DEVICE DELIVERED IN A FASTER THAN EXPECTED TIME DURING A PATIENT INFUSION. THE PUMP FULLY INFUSED A SOLUTION OF 8 GRAMS OF FLUCLOXACILLIN AND 240ML OF NORMAL SALINE 2-3 HOURS EARLIER THAN INTENDED. THERE WAS NO REPORT OF PATIENT INJURY, MEDICAL INTERVENTION NECESSARY, OR ADVERSE REACTION IN ASSOCIATION WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CE INFUSOR LV10, 12 PACK | PUMP, INFUSION, ELASTOMERIC | MEB | BAXTER HEALTHCARE - IRVINE | 10C057 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |