MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,study report with the FDA on 2020-02-14 for UNK PATELLA HANDLE/CLAMP manufactured by Depuy Orthopaedics Inc Us.
[179438332]
(b)(4). If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10
[179438333]
Clinical adverse event received for retained foreign body right knee : head of attune patella clamp. Event is serious and is considered severe. Event is definitely related to both device and procedure. Date of implantation: (b)(6) 2019. Date of event (onset): (b)(6) 2020 (right knee).
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1818910-2020-04863 |
MDR Report Key | 9711323 |
Report Source | HEALTH PROFESSIONAL,STUDY |
Date Received | 2020-02-14 |
Date of Report | 2020-01-28 |
Date of Event | 2020-01-08 |
Date Mfgr Received | 2020-03-20 |
Date Added to Maude | 2020-02-14 |
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 | KARA DITTY-BOVARD |
Manufacturer Street | 700 ORTHOPAEDIC DRIVE |
Manufacturer City | WARSAW IN 465810988 |
Manufacturer Country | US |
Manufacturer Postal | 465810988 |
Manufacturer Phone | 6107428552 |
Manufacturer G1 | DEPUY ORTHOPAEDICS, INC. 1818910 |
Manufacturer Street | 700 ORTHOPAEDIC DR. |
Manufacturer City | WARSAW IN 465810988 |
Manufacturer Country | US |
Manufacturer Postal Code | 465810988 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | UNK PATELLA HANDLE/CLAMP |
Generic Name | PATELLA HANDLE/CLAMP |
Product Code | HXD |
Date Received | 2020-02-14 |
Catalog Number | UNK PATELLA HANDLE/CLAMP |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DEPUY ORTHOPAEDICS INC US |
Manufacturer Address | 700 ORTHOPAEDIC DRIVE WARSAW IN 465810988 US 465810988 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-02-14 |