MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-02-28 for SMITHS MEDICAL PORTEX COMBINED SPINAL EPIDURAL TRAY A3307-17 manufactured by Smiths Medical Asd, Inc..
[181408065]
Information was received that a smiths medical epidural tray had a hole in the side wall of the catheter and fluid was noted to have leaked out. No adverse effects reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3012307300-2020-01608 |
MDR Report Key | 9770052 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2020-02-28 |
Date of Report | 2020-03-31 |
Date Mfgr Received | 2020-03-31 |
Date Added to Maude | 2020-02-28 |
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 | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | DAVE HALVERSON |
Manufacturer Street | 6000 NATHAN LANE N |
Manufacturer City | MINNEAPOLIS, MN |
Manufacturer Country | US |
Manufacturer G1 | SMITHS MEDICAL ASD, INC. |
Manufacturer Street | 10 BOWMAN DRIVE |
Manufacturer City | KEENE, NH |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SMITHS MEDICAL PORTEX COMBINED SPINAL EPIDURAL TRAY |
Generic Name | SPINAL EPIDURAL ANESTHESIA KIT |
Product Code | OFT |
Date Received | 2020-02-28 |
Catalog Number | A3307-17 |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITHS MEDICAL ASD, INC. |
Manufacturer Address | 6000 NATHAN LANE N MINNEAPOLIS, MN US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-28 |