MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-03-31 for HUDSON/MODIFIED TRINKLE REAMER 4100235000 manufactured by Stryker Instruments-kalamazoo.
[186727046]
The device disassembled during inspection at the manufacturer facility.? There were no adverse consequences related to this event.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 0001811755-2020-00817 |
MDR Report Key | 9903127 |
Report Source | USER FACILITY |
Date Received | 2020-03-31 |
Date of Report | 2020-03-31 |
Date of Event | 2020-03-12 |
Date Mfgr Received | 2020-03-12 |
Device Manufacturer Date | 2014-02-03 |
Date Added to Maude | 2020-03-31 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. ZACH BAKER |
Manufacturer Street | 4100 EAST MILHAM AVENUE |
Manufacturer City | KALAMAZOO MI 49001 |
Manufacturer Country | US |
Manufacturer Postal | 49001 |
Manufacturer Phone | 2693237700 |
Manufacturer G1 | STRYKER INSTRUMENTS-KALAMAZOO |
Manufacturer Street | 4100 EAST MILHAM AVENUE |
Manufacturer City | KALAMAZOO MI 49001 |
Manufacturer Country | US |
Manufacturer Postal Code | 49001 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HUDSON/MODIFIED TRINKLE REAMER |
Generic Name | ARTHROSCOPE |
Product Code | HRX |
Date Received | 2020-03-31 |
Model Number | 4100235000 |
Catalog Number | 4100235000 |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | STRYKER INSTRUMENTS-KALAMAZOO |
Manufacturer Address | 4100 EAST MILHAM AVENUE KALAMAZOO MI 49001 US 49001 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-31 |