MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1997-10-16 for UNK manufactured by Burlington Medical Supplies.
[101805]
Facility notified of recall by mfr and advised to check the lead aprons for contamination. Aprons were checked and found to be contaminated. Aprons returned to mfr.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1012284 |
| MDR Report Key | 126513 |
| Date Received | 1997-10-16 |
| Date of Report | 1997-10-16 |
| Date of Event | 1997-09-24 |
| Date Added to Maude | 1997-10-20 |
| 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 | UNK |
| Generic Name | LEAD APRONS |
| Product Code | EAJ |
| Date Received | 1997-10-16 |
| Returned To Mfg | 1997-10-15 |
| Model Number | UNK |
| Catalog Number | UNK |
| Lot Number | UNK |
| ID Number | LW601 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 123819 |
| Manufacturer | BURLINGTON MEDICAL SUPPLIES |
| Manufacturer Address | 3 ELMHURST ST NEWPORT NEWS VA 23603 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1997-10-16 |