MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-03-07 for ACTIVE HEEL TRACTION BOOT 72202682 manufactured by Smith & Nephew, Inc..
[138289922]
(b)(6).
Patient Sequence No: 1, Text Type: N, H10
[138289923]
It was reported that during hip arthroscopy, the boot plastic frame cracked. The procedure was successfully completed using a back-up device. A delay between 30 and 60 minutes was reported. No patient injury or other complications were reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3003604053-2019-00028 |
MDR Report Key | 8401264 |
Date Received | 2019-03-07 |
Date of Report | 2019-06-24 |
Date of Event | 2019-02-25 |
Date Mfgr Received | 2019-06-21 |
Date Added to Maude | 2019-03-07 |
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 | JIM GONZALES |
Manufacturer Street | 7000 WEST WILLIAM CANNON DRIVE |
Manufacturer City | AUSTIN TX 78735 |
Manufacturer Country | US |
Manufacturer Postal | 78735 |
Manufacturer Phone | 5123585706 |
Manufacturer G1 | SMITH & NEPHEW, INC. |
Manufacturer Street | 150 MINUTEMAN ROAD |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal Code | 01810 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | ACTIVE HEEL TRACTION BOOT |
Generic Name | APPARATUS, TRACTION, NON-POWERED |
Product Code | HST |
Date Received | 2019-03-07 |
Catalog Number | 72202682 |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITH & NEPHEW, INC. |
Manufacturer Address | 150 MINUTEMAN ROAD ANDOVER MA 01810 US 01810 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-03-07 |