MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-17 for AUTOPLEX 0607687000 manufactured by Stryker Corp..
[175917695]
Stryker cement mixer cannula would not connect after cement mixed.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5092354 |
| MDR Report Key | 9610677 |
| Date Received | 2020-01-17 |
| Date of Report | 2020-01-16 |
| Date of Event | 2019-12-18 |
| Date Added to Maude | 2020-01-21 |
| 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 | 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 | AUTOPLEX |
| Generic Name | CEMENT MIXER, FOR CLINICAL USE |
| Product Code | JDZ |
| Date Received | 2020-01-17 |
| Catalog Number | 0607687000 |
| Lot Number | 19155012 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | STRYKER CORP. |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-01-17 |