MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2003-10-30 for BARRIER EXTRA PROTECTION SURGICAL GOWN, EXTRA LARGE 0576 manufactured by Molnlycke Health Care Ab.
[329826]
Scrub nurse reported experiencing "strikethrough" in the leg area of the gown.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2523357-2003-00007 |
MDR Report Key | 493328 |
Report Source | 05,06 |
Date Received | 2003-10-30 |
Date of Report | 2003-10-30 |
Date of Event | 2003-07-31 |
Date Mfgr Received | 2003-09-29 |
Date Added to Maude | 2003-11-05 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Manufacturer Contact | JOHN CLAY |
Manufacturer Street | 826 NEWTOWN-YARDLEY RD. |
Manufacturer City | NEWTOWN PA 18940 |
Manufacturer Country | US |
Manufacturer Postal | 18940 |
Manufacturer Phone | 8008824582 |
Manufacturer G1 | * |
Manufacturer Street | 160 MOO 17 BANGPLEE IND. BANGNA-TRAD RD KM 23, SAMUTPRA |
Manufacturer City | TAMBOL HANGSAOTHONG |
Manufacturer Country | TH |
Single Use | 3 |
Remedial Action | OT |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BARRIER EXTRA PROTECTION SURGICAL GOWN, EXTRA LARGE |
Generic Name | GOWN, SURGICAL |
Product Code | FYE |
Date Received | 2003-10-30 |
Model Number | NA |
Catalog Number | 0576 |
Lot Number | UNK |
ID Number | UNK |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 482033 |
Manufacturer | MOLNLYCKE HEALTH CARE AB |
Manufacturer Address | BOX 13080 GOTEBORG SW SE-402 52 |
Baseline Brand Name | BARRIER SURGICAL GOWN |
Baseline Generic Name | GOWN, SURGICAL |
Baseline Catalog No | 0576 |
Baseline ID | 9676 |
Baseline Device Family | SURGICAL GOWNS |
Baseline Shelf Life Contained | Y |
Baseline Shelf Life [Months] | 60 |
Baseline PMA Flag | N |
Baseline 510K PMN | Y |
Premarket Notification | K760903 |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2003-10-30 |