MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-19 for DYNJ0151441C manufactured by Medline Industries Inc..
| Report Number | 1423395-2019-00029 |
| MDR Report Key | 8907344 |
| Date Received | 2019-08-19 |
| Date of Report | 2019-08-19 |
| Date of Event | 2019-07-25 |
| Date Mfgr Received | 2019-08-12 |
| Date Added to Maude | 2019-08-19 |
| 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 | 3 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | NIGEL VILCHES |
| Manufacturer Street | THREE LAKES DRIVE |
| Manufacturer City | NORTHFIELD IL 600932753 |
| Manufacturer Country | US |
| Manufacturer Postal | 600932753 |
| Manufacturer Phone | 2249311458 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Generic Name | SURGICAL BLADE IN HAND AND FOOT PACK-LF |
| Product Code | OJH |
| Date Received | 2019-08-19 |
| Returned To Mfg | 2019-08-14 |
| Catalog Number | DYNJ0151441C |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDLINE INDUSTRIES INC. |
| Manufacturer Address | THREE LAKES DRIVE NORTHFIELD IL 600932753 US 600932753 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2019-08-19 |