MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-06-14 for 401261 401261RR manufactured by Stryker Sustainability Solutions Phoenix.
Report Number | 0002090040-2019-00018 |
MDR Report Key | 8700415 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2019-06-14 |
Date of Report | 2019-06-14 |
Date of Event | 2019-04-12 |
Date Mfgr Received | 2019-05-23 |
Device Manufacturer Date | 2019-01-28 |
Date Added to Maude | 2019-06-14 |
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 | MR. MARISSA RICHMOND |
Manufacturer Street | 1810 W. DRAKE DRIVE |
Manufacturer City | TEMPE AZ 85283 |
Manufacturer Country | US |
Manufacturer Postal | 85283 |
Manufacturer Phone | 8888883433 |
Manufacturer G1 | STRYKER SUSTAINABILITY SOLUTIONS PHOENIX |
Manufacturer Street | 10232 S. 51ST ST. |
Manufacturer City | PHOENIX AZ 85044 |
Manufacturer Country | US |
Manufacturer Postal Code | 85044 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NA |
Generic Name | CATHETER, RECORDING, ELECTRODE, REPROCESSED |
Product Code | NLH |
Date Received | 2019-06-14 |
Returned To Mfg | 2019-04-19 |
Model Number | 401261 |
Catalog Number | 401261RR |
Lot Number | 3799744 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | STRYKER SUSTAINABILITY SOLUTIONS PHOENIX |
Manufacturer Address | 10232 S. 51ST ST. PHOENIX AZ 85044 US 85044 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-06-14 |