MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2002-09-16 for BLUE NEOPRENE BAG 3L 78300APEX manufactured by Rusch Inc. Manufacturing (uk).
[15484867]
Bag burst.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 8010092-2002-00189 |
MDR Report Key | 418220 |
Report Source | 08 |
Date Received | 2002-09-16 |
Date of Report | 2002-09-12 |
Date Mfgr Received | 2002-09-12 |
Date Added to Maude | 2002-09-26 |
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 | 0 |
Manufacturer Contact | ROLANDA SCOTT, DOCUMENT CONTROL |
Manufacturer Street | 2450 MEADOWBROOK PARKWAY |
Manufacturer City | DULUTH GA 30136 |
Manufacturer Country | US |
Manufacturer Postal | 30136 |
Manufacturer Phone | 7706230816 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BLUE NEOPRENE BAG 3L |
Generic Name | ANESTHESIA |
Product Code | BYW |
Date Received | 2002-09-16 |
Model Number | NA |
Catalog Number | 78300APEX |
Lot Number | UNK |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 407256 |
Manufacturer | RUSCH INC. MANUFACTURING (UK) |
Manufacturer Address | PORTADOWN RD., LURGAN CRAIGAVON CO. ARMAGH, N. IRELAND UK BT66 8RD |
Baseline Brand Name | BLUE NEOPRENE BAG |
Baseline Generic Name | NA |
Baseline Model No | NA |
Baseline Catalog No | 78300APEX |
Baseline ID | NA |
Baseline Device Family | ENTERAL |
Baseline Shelf Life Contained | N |
Baseline Shelf Life [Months] | * |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | Y |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2002-09-16 |