MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2003-03-21 for REBREATHING BAG 2707202 manufactured by Rusch Manufacturing (uk).
[265587]
Customer reports bag ripped during use.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 8010092-2003-00038 |
MDR Report Key | 450690 |
Report Source | 06 |
Date Received | 2003-03-21 |
Date of Report | 2003-03-14 |
Date Mfgr Received | 2003-03-11 |
Date Added to Maude | 2003-04-01 |
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 | ROLANDA SCOTT, COORDINATOR |
Manufacturer Street | 2450 MEADOWBROOK PARKWAY |
Manufacturer City | DULUTH GA 30136 |
Manufacturer Country | US |
Manufacturer Postal | 30136 |
Manufacturer Phone | 7706230816 |
Manufacturer G1 | RUSCH, INC. |
Manufacturer Street | 2450 MEADOWBROOK PARKWAY |
Manufacturer City | DULUTH GA 30136 |
Manufacturer Country | US |
Manufacturer Postal Code | 30136 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | REBREATHING BAG |
Generic Name | ANESTHESIA |
Product Code | BYW |
Date Received | 2003-03-21 |
Model Number | NA |
Catalog Number | 2707202 |
Lot Number | UNK |
ID Number | NA |
Operator | LAY USER/PATIENT |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 439683 |
Manufacturer | RUSCH MANUFACTURING (UK) |
Manufacturer Address | PORTADOWN RD., LURGAN CRAIGAVON CO. ARMAGH, N. IRELAND UK BT66 8RD |
Baseline Brand Name | REBREATHING BAG |
Baseline Generic Name | ANESTHESIA |
Baseline Model No | NA |
Baseline Catalog No | 2707202 |
Baseline ID | NA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2003-03-21 |