INFUSOR
Report
- Report Number
- 1416980-2020-03970
- Event Type
- Malfunction
- Date Received
- July 14, 2020
- Date of Event
- June 19, 2020
- Report Date
- August 18, 2020
- Manufacturer
- BAXTER HEALTHCARE CORPORATION
- Product Code
- MEB
- UDI-DI
- 00085412081366
- PMA / PMN Number
- K071222
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AS
- Reporter Occupation
- NURSE
Narratives
CORRECTION MADE TO G5: PMA/510K #: K071222 (PREVIOUSLY NA). ADDITIONAL INFORMATION WAS ADDED TO H4 AND H6. H4: THE LOT WAS MANUFACTURED FROM NOVEMBER 25, 2019 - NOVEMBER 26, 2019. H10: A BATCH REVIEW WAS CONDUCTED AND THERE WERE NO DEVIATIONS FOUND RELATED TO THIS REPORTED CONDITION DURING THE MANUFACTURE OF THIS LOT. THE DEVICE WAS NOT RECEIVED FOR EVALUATION; THEREFORE, A DEVICE ANALYSIS COULD NOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
(B)(6). SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
IT WAS REPORTED THAT A LARGE VOLUME INFUSOR UNDER INFUSED. IT WAS FURTHER REPORTED APPROXIMATELY 30 - 40% OF THE SOLUTION REMAINED IN THE DEVICE. THE DEVICE HAD BEEN FILLED WITH 18000MG PIPERACILLIN / TAZOBACTAM DILUTED IN 0.9% SODIUM CHLORIDE AND WAS INFUSED VIA A PICC (PERIPHERALLY INSERTED CENTRAL CATHETER).. THERE WAS NO REPORT OF PATIENT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS EVENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 733888 | INFUSOR | PUMP, INFUSION, ELASTOMERIC | MEB | BAXTER HEALTHCARE CORPORATION | NA | 19M041 | 00085412081366 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | PICC LINE| PIPERACILLIN / TAZOBACTAM 18000MG| SODIUM CHLORIDE 0.9%| PICC LINE| PIPERACILLIN / TAZOBACTAM 18000MG| SODIUM CHLORIDE 0.9% |