MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,05,06,07 report with the FDA on 2000-08-17 for PERCUPUMP CT INJECTOR WITH EDA 7805 manufactured by E-z-em, Inc..
[167214]
The injector was set to inject a total volume of 143ml of contrast in antecubital fossa. It was reported that the contrast was visible after injection and, upon examining the pt, an extravasation of approximately 135cc was observed. The extravasation was uniformly spread out from the wrist to the elbow and was hard and firm (blood flow was not restricted). The pt did not complain of pain and no redness was noted. Pt was treated with ice and the arm was kept elevated. Pt was kept in the dept for approximately 1 hour for observation.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2432460-2000-00026 |
| MDR Report Key | 291720 |
| Report Source | 00,05,06,07 |
| Date Received | 2000-08-17 |
| Date of Report | 2000-07-12 |
| Date of Event | 2000-07-11 |
| Date Facility Aware | 2000-07-11 |
| Report Date | 2000-07-12 |
| Date Reported to Mfgr | 2000-07-12 |
| Date Mfgr Received | 2000-07-12 |
| Device Manufacturer Date | 1998-03-01 |
| Date Added to Maude | 2000-08-24 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | PETER APRILE, R.PH. |
| Manufacturer Street | 717 MAIN ST |
| Manufacturer City | WESTBURY NY 11590 |
| Manufacturer Country | US |
| Manufacturer Postal | 11590 |
| Manufacturer Phone | 8005444624 |
| Manufacturer G1 | * |
| Manufacturer Street | * |
| Manufacturer City | * |
| Manufacturer Country | * |
| Single Use | 3 |
| Remedial Action | PM |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PERCUPUMP CT INJECTOR WITH EDA |
| Generic Name | CT INJECTOR WITH EXTRAVASATION ACCESSORY |
| Product Code | FIH |
| Date Received | 2000-08-17 |
| Model Number | NA |
| Catalog Number | 7805 |
| Lot Number | NA |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | 28 MO |
| Device Eval'ed by Mfgr | R |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 282341 |
| Manufacturer | E-Z-EM, INC. |
| Manufacturer Address | 113-117 MAGNOLIA AVE. WESTBURY NY 11590 US |
| Baseline Brand Name | PERCUPUMP TOUCHSCREEN INJECTOR W/EDA |
| Baseline Generic Name | CT INJECTOR SYSTEM |
| Baseline Model No | NA |
| Baseline Catalog No | 7805 |
| Baseline ID | NA |
| Baseline Device Family | PERCUPUMP INJECTOR SYSTEM |
| Baseline Shelf Life [Months] | NA |
| Baseline PMA Flag | N |
| Baseline 510K PMN | Y |
| Premarket Notification | K961845 |
| Baseline Preamendment | N |
| Baseline Transitional | N |
| 510k Exempt | N |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 1 | 1. Other | 2000-08-17 |