FDA Adverse Event
Injury
Summary report: N
MAXI MOVE
MDR report key: 3938555
·
Received June 27, 2014
Report
- Report Number
- 9681684-2014-00043
- Event Type
- Injury
- Date Received
- June 27, 2014
- Manufacturer
- ARJOHUNTLEIGH MAGOG INC.
- Product Code
- FSA
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
THIS REPORT IS BEING FILED UNDER EXEMPTION (B)(4) BY THE MANUFACTURER ARJOHUNTLEIGH MAGOG INC. ((B)(4)) ON BEHALF OF THE IMPORTER ARJOHUNTLEIGH INC (AHUS) ((B)(4)). ADDITIONAL INFORMATION WILL BE PROVIDED FOLLOWING THE CONCLUSION OF THE MANUFACTURER'S INVESTIGATION.
Description of Event or Problem · 1
(B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 375729 | MAXI MOVE | FSA | ARJOHUNTLEIGH MAGOG INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |