MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2018-04-24 for REBOUND AIR WALKER MD B-242900003 manufactured by Ossur Americas, Inc..
[106330897]
Patient claim of pressure and swelling on tendons while wearing orthopedic walking boot.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2085446-2018-00001 |
MDR Report Key | 7455123 |
Report Source | DISTRIBUTOR |
Date Received | 2018-04-24 |
Date of Report | 2018-04-24 |
Date Mfgr Received | 2018-03-27 |
Date Added to Maude | 2018-04-24 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MRS. CRYSTAL SWAFFORD |
Manufacturer Street | 27051 TOWNE CENTRE |
Manufacturer City | FOOTHILL RANCH CA 92610 |
Manufacturer Country | US |
Manufacturer Postal | 92610 |
Manufacturer Phone | 9493823817 |
Manufacturer G1 | OSSUR AMERICAS, INC. |
Manufacturer Street | 27051 TOWNE CENTRE |
Manufacturer City | FOOTHILL RANCH CA 92610 |
Manufacturer Country | US |
Manufacturer Postal Code | 92610 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | REBOUND AIR WALKER MD |
Generic Name | JOINT, ANKLE, EXTERNAL BRACE |
Product Code | ITW |
Date Received | 2018-04-24 |
Returned To Mfg | 2018-03-27 |
Model Number | B-242900003 |
Catalog Number | B-242900003 |
Operator | LAY USER/PATIENT |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | OSSUR AMERICAS, INC. |
Manufacturer Address | 27051 TOWNE CENTRE FOOTHILL RANCH CA 92610 US 92610 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2018-04-24 |