MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1997-10-08 for MOBILE SHIELD UNK 62531 manufactured by Bar-ray Products, Inc..
[113315]
User tested the product with the pancake probe (geiger counter) and found it to be contaminated as evidenced by a reading of. 5 mr/hr.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1012251 |
| MDR Report Key | 125210 |
| Date Received | 1997-10-08 |
| Date of Report | 1997-10-08 |
| Date of Event | 1997-10-07 |
| Date Added to Maude | 1997-10-10 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| 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 | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | MOBILE SHIELD |
| Generic Name | * |
| Product Code | IWQ |
| Date Received | 1997-10-08 |
| Model Number | UNK |
| Catalog Number | 62531 |
| Lot Number | UNK |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 122575 |
| Manufacturer | BAR-RAY PRODUCTS, INC. |
| Manufacturer Address | 95 MONARCH ST. LITTLETOWN PA 17340 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1997-10-08 |