MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-09-13 for ADJUSTAFIT BOOT AL056003 manufactured by Breg, Inc..
[86282936]
Product not available for evaluation. Investigation of issue already completed resulting in a negligible incidence rate. Manufacturing process improvement already implemented to prevent recurrence.
Patient Sequence No: 1, Text Type: N, H10
[86282937]
Reported incident of sole separating from boot. No report of injury involved with incident.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2028253-2017-00075 |
MDR Report Key | 6863411 |
Date Received | 2017-09-13 |
Date of Report | 2017-09-11 |
Date Mfgr Received | 2017-08-21 |
Date Added to Maude | 2017-09-13 |
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 | 0 |
Initial Report to FDA | 0 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MRS. CAROL EMERSON |
Manufacturer Street | 2885 LOKER AVENUE EAST |
Manufacturer City | CARLSBAD CA 92010 |
Manufacturer Country | US |
Manufacturer Postal | 92010 |
Manufacturer Phone | 7607955823 |
Manufacturer G1 | BREG, INC. |
Manufacturer Street | 2885 LOKER AVENUE EAST |
Manufacturer City | CARLSBAD CA 92010 |
Manufacturer Country | US |
Manufacturer Postal Code | 92010 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | ADJUSTAFIT BOOT |
Generic Name | ADJUSTAFIT BOOT |
Product Code | IQI |
Date Received | 2017-09-13 |
Model Number | AL056003 |
Catalog Number | AL056003 |
Operator | LAY USER/PATIENT |
Device Availability | * |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BREG, INC. |
Manufacturer Address | 2885 LOKER AVENUE EAST CARLSBAD CA 92010 US 92010 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2017-09-13 |