MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-17 for TRANSCYTE manufactured by Organogenesis, Inc..
[183741325]
Transcyte used on several patients. Notified by the vendor some of our product was expired. Product has inner component and outer wrapper. Both dates are different.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9840585 |
| MDR Report Key | 9840585 |
| Date Received | 2020-03-17 |
| Date of Report | 2020-03-09 |
| Date of Event | 2020-02-21 |
| Report Date | 2020-03-09 |
| Date Reported to FDA | 2020-03-09 |
| Date Reported to Mfgr | 2020-03-17 |
| Date Added to Maude | 2020-03-17 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | TRANSCYTE |
| Generic Name | DRESSING, WOUND AND BURN, INTERACTIVE |
| Product Code | MGR |
| Date Received | 2020-03-17 |
| Lot Number | 150468; 150436; 150527 |
| Device Availability | * |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ORGANOGENESIS, INC. |
| Manufacturer Address | 10933 NORTH TORREY PINES ROAD LA JOLLA CA 92037 US 92037 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-17 |