FDA Adverse Event
Other
Summary report: N
ACE
MDR report key: 313727
·
Received January 23, 2001
Report
- Report Number
- 1526439-2001-00001
- Event Type
- Other
- Date Received
- January 23, 2001
- Report Date
- January 23, 2001
- Manufacturer
- DEPUY ACROMED, INC.
- Product Code
- HAX
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED TO DEPUY ACROMED THAT AN ACE SPRING PIN WAS NOT FUNCTIONING PROPERLY. THE PRODUCT HAS BEEN RETURNED AND IS CURRENTLY BEING EVALUATED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2784 | ACE | SPRING PIN | HAX | DEPUY ACROMED, INC. | NA | 0698W |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Other |