MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1996-02-14 for ARTHROSCOPE 275-756-000 manufactured by Stryker Endoscopy Div. Stryker Corp..
[17376]
Possible product problem; during arthroscopy, a small piece of metal was seen. Rptr questions if it breaks off from knee shaver. 3 possible boxes with 3 (packaging not saved). 1. 95096352, 2. 96015012, 3. 93126682.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1008332 |
| MDR Report Key | 30211 |
| Date Received | 1996-02-14 |
| Date of Report | 1996-02-11 |
| Date of Event | 1996-01-22 |
| Date Added to Maude | 1996-02-20 |
| 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 | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ARTHROSCOPE |
| Generic Name | ARTHROSCOPE |
| Product Code | LLO |
| Date Received | 1996-02-14 |
| Catalog Number | 275-756-000 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 30933 |
| Manufacturer | STRYKER ENDOSCOPY DIV. STRYKER CORP. |
| Manufacturer Address | SAN JOSE CA 95134 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1996-02-14 |