MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2004-03-02 for BREATHING BAG 2107202 manufactured by Rusch U.k Ltd.
[20759126]
Customer reports hole in bag.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 8010092-2004-00023 |
| MDR Report Key | 530848 |
| Report Source | 08 |
| Date Received | 2004-03-02 |
| Date of Report | 2004-03-01 |
| Date Mfgr Received | 2004-02-20 |
| Date Added to Maude | 2004-06-23 |
| 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 PKWY |
| 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 | BREATHING BAG |
| Generic Name | ANESTHESIA |
| Product Code | BYW |
| Date Received | 2004-03-02 |
| Model Number | NA |
| Catalog Number | 2107202 |
| Lot Number | BW28 |
| 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 | 520096 |
| Manufacturer | RUSCH U.K LTD |
| Manufacturer Address | PORTADOWN RD. N. IRELAND UK BT66 8RD |
| Baseline Brand Name | BREATHING BAG |
| Baseline Generic Name | ANESTHESIA |
| Baseline Model No | NA |
| Baseline Catalog No | 2107202 |
| Baseline ID | NA |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2004-03-02 |