MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-10 for HALYARD GOWN SURG NON-REINFORCED 72888 manufactured by Halyard Health.
Report Number | 3014527682-2020-00003 |
MDR Report Key | 9813683 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-03-10 |
Date of Report | 2020-03-10 |
Date of Event | 2019-07-22 |
Date Mfgr Received | 2019-07-27 |
Date Added to Maude | 2020-03-10 |
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 | MRS. CHEYENNE STEWART |
Manufacturer Street | 3000 EAST SAWYER ROAD |
Manufacturer City | REPUBLIC MO 65738 |
Manufacturer Country | US |
Manufacturer Postal | 65738 |
Manufacturer Phone | 4177303937 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HALYARD GOWN SURG NON-REINFORCED |
Generic Name | HALYARD GOWN SURG NON-REINFORCED |
Product Code | FYA |
Date Received | 2020-03-10 |
Catalog Number | 72888 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | HALYARD HEALTH |
Manufacturer Address | ALPHARETTA GA US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-10 |