MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-19 for OSTEORAPTOR UNKNOWN manufactured by Smith & Nephew, Inc..
[184271785]
(b)(6).
Patient Sequence No: 1, Text Type: N, H10
[184271786]
A surgeon has reported using a curved osteroraptor device during surgery for shoulder stabilization. Post-operatively surgeon noted an unidentified small fragment of metal in the shoulder. No further information was reported. It is unknown if piece of metal came from the osteoraptor introducer. All available information has been disclosed. If additional information should become available, a supplemental report will be submitted accordingly.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1219602-2020-00537 |
MDR Report Key | 9857602 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-19 |
Date of Report | 2020-03-19 |
Date of Event | 2020-02-24 |
Date Mfgr Received | 2020-02-24 |
Date Added to Maude | 2020-03-19 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | HOLLY TOPPING |
Manufacturer Street | 7000 WEST WILLIAM CANNON DRIVE |
Manufacturer City | AUSTIN TX 78735 |
Manufacturer Country | US |
Manufacturer Postal | 78735 |
Manufacturer Phone | 5123913905 |
Manufacturer G1 | SMITH & NEPHEW, INC. |
Manufacturer Street | 130 FORBES BOULEVARD |
Manufacturer City | MANSFIELD MA 02048 |
Manufacturer Country | US |
Manufacturer Postal Code | 02048 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | OSTEORAPTOR |
Generic Name | FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE |
Product Code | MAI |
Date Received | 2020-03-19 |
Catalog Number | UNKNOWN |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITH & NEPHEW, INC. |
Manufacturer Address | 130 FORBES BOULEVARD MANSFIELD MA 02048 US 02048 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-19 |