MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2004-12-27 for HHP HAND HELD BAR CODE SCANNER VT3060 8902114 manufactured by Hand Held Products Inc.
[569279]
The hhp wand scanner on the oas server misread sample bar code labels on three different occasions. No death or serious injury was associated with the incident.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2250051-2004-02936 |
| MDR Report Key | 810094 |
| Date Received | 2004-12-27 |
| Date of Report | 2004-12-27 |
| Date of Event | 2004-12-07 |
| Date Added to Maude | 2007-01-31 |
| Event Key | 0 |
| Report Source Code | Distributor report |
| Manufacturer Link | N |
| 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 | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | HHP HAND HELD BAR CODE SCANNER |
| Generic Name | HAND-HELD LED UNIT |
| Product Code | LRH |
| Date Received | 2004-12-27 |
| Model Number | VT3060 |
| Catalog Number | 8902114 |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 797578 |
| Manufacturer | HAND HELD PRODUCTS INC |
| Manufacturer Address | 700 VISIONS DR SKANEATELES FALLS NY 131530208 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2004-12-27 |