MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-13 for VASOPRESS DIGITAL PUMP VP500D manufactured by Compression Therapy Concepts, Inc..
Report Number | 3002834373-2019-00002 |
MDR Report Key | 9028307 |
Date Received | 2019-09-13 |
Date of Report | 2019-09-13 |
Date Mfgr Received | 2019-09-12 |
Date Added to Maude | 2019-09-13 |
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 | 3 |
Reporter Occupation | BIOMEDICAL ENGINEER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. CHRISTINA ARNT |
Manufacturer Street | 56 E. BELL DRIVE |
Manufacturer City | WARSAW IN 46580 |
Manufacturer Country | US |
Manufacturer Postal | 46580 |
Manufacturer Phone | 5745273773 |
Manufacturer G1 | COMPRESSION THERAPY CONCEPTS, INC. |
Manufacturer Street | 555 INDUSTRIAL WAY W |
Manufacturer City | EATONTOWN NJ 07724 |
Manufacturer Country | US |
Manufacturer Postal Code | 07724 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | N/A |
Event Type | 3 |
Type of Report | 0 |
Brand Name | VASOPRESS DIGITAL PUMP |
Generic Name | SLEEVE, LIMB, COMPRESSIBLE |
Product Code | JOW |
Date Received | 2019-09-13 |
Returned To Mfg | 2019-05-23 |
Catalog Number | VP500D |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COMPRESSION THERAPY CONCEPTS, INC. |
Manufacturer Address | 555 INDUSTRIAL WAY W EATONTOWN NJ 07724 US 07724 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-09-13 |