MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1999-08-31 for POSEY 5608 * manufactured by J.t. Posey Co.
[160074]
A posey palm cone was placed in the hand of an 89 yr old resident with a long-standing >14 year flexure contracture of the left hand. Within a short period of time, (hrs) she developed a stage iii wound on left thumb and hand.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 238516 |
MDR Report Key | 238516 |
Date Received | 1999-08-31 |
Date of Report | 1999-08-30 |
Date of Event | 1999-08-20 |
Date Facility Aware | 1999-08-20 |
Report Date | 1999-08-30 |
Date Reported to FDA | 1999-08-31 |
Date Reported to Mfgr | 1999-08-31 |
Date Added to Maude | 1999-09-07 |
Event Key | 0 |
Report Source Code | User Facility 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 | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | POSEY |
Generic Name | PALM CONE |
Product Code | ILH |
Date Received | 1999-08-31 |
Model Number | 5608 |
Catalog Number | * |
Lot Number | * |
ID Number | TH16956087 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | 14 DAY |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 231118 |
Manufacturer | J.T. POSEY CO |
Manufacturer Address | 5635 PECK RD ARCADIA CA 91006 US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1999-08-31 |