MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2017-01-31 for SR MCP, IMPLANT SIZE MEDIUM 5800MD00 manufactured by Stryker Gmbh.
[66125028]
(b)(4). Device will not be returned. If additional information becomes available it will be provided on a supplemental report. Patient keep the device.
Patient Sequence No: 1, Text Type: N, H10
[66125029]
The silicone part of the joint perforated through the bone towards the palm arm. The joint slipped off and had to be extracted and replaced
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 0008031020-2017-00052 |
| MDR Report Key | 6289144 |
| Report Source | OTHER |
| Date Received | 2017-01-31 |
| Date of Report | 2018-01-19 |
| Date of Event | 2016-09-08 |
| Date Mfgr Received | 2018-01-12 |
| Device Manufacturer Date | 2012-03-14 |
| Date Added to Maude | 2017-01-31 |
| 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. ANNA JUSINSKI |
| Manufacturer Street | 325 CORPORATE DRIVE |
| Manufacturer City | MAHWAH NJ 07430 |
| Manufacturer Country | US |
| Manufacturer Postal | 07430 |
| Manufacturer Phone | 2018315000 |
| Manufacturer G1 | STRYKER GMBH |
| Manufacturer Street | BOHNACKERWEG 1 POSTFACH |
| Manufacturer City | SELZACH 2545 |
| Manufacturer Country | CH |
| Manufacturer Postal Code | 2545 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | SR MCP, IMPLANT SIZE MEDIUM |
| Generic Name | SEMI-CONSTRAINED METAL/POLYMER FINGER JOINT PROSTHESIS |
| Product Code | MPK |
| Date Received | 2017-01-31 |
| Catalog Number | 5800MD00 |
| Lot Number | 22847801 |
| Device Expiration Date | 2016-12-31 |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | STRYKER GMBH |
| Manufacturer Address | BOHNACKERWEG 1 POSTFACH SELZACH 2545 CH 2545 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2017-01-31 |