MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2003-07-22 for POSEY PREEMIE REMOVABLE ID 4649 * manufactured by J T Posey Company.
[21691286]
Preemie removable "posey" i. D. Band used on pt to left ankle. Right foot had several surface scratches and 3 different small "pin-dot" areas of puncture, smear of blood noted on edges of band. The edges of i. D. Band under white posey label noted to be very hard and sharp. Neosporin applied to foot without band removed.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1029274 |
| MDR Report Key | 477813 |
| Date Received | 2003-07-22 |
| Date of Report | 2003-07-21 |
| Date of Event | 2003-07-12 |
| Date Added to Maude | 2003-08-18 |
| 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 | POSEY PREEMIE REMOVABLE ID |
| Generic Name | REMOVABLE ID BAND |
| Product Code | LDQ |
| Date Received | 2003-07-22 |
| Returned To Mfg | 2003-06-21 |
| Model Number | 4649 |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 466621 |
| Manufacturer | J T POSEY COMPANY |
| Manufacturer Address | 3635 PECK ROAD ARCADIA CA 91006 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2003-07-22 |