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 |