MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2020-01-28 for PROSTHESIS, ELBOW, HEMI-, RADIAL - NECK manufactured by Acumedllc.
[183717321]
Additional mdrs associated with this event: 3025141-2020-00022: head, 3025141-2020-00024: stem.
Patient Sequence No: 1, Text Type: N, H10
[183717322]
Patient received a arh slide loc radial head replacement system in 2017. X-ray shows that the head/neck construct appears to be dissociated from the stem. Revision surgery has not been scheduled to date.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3025141-2020-00023 |
MDR Report Key | 9637563 |
Report Source | DISTRIBUTOR |
Date Received | 2020-01-28 |
Date of Report | 2020-01-21 |
Date Mfgr Received | 2020-01-21 |
Date Added to Maude | 2020-01-28 |
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 | MS. MICKI ANDERSON |
Manufacturer Street | 5885 NE CORNELIUS PASS ROAD |
Manufacturer City | HILLSBORO OR 97124 |
Manufacturer Country | US |
Manufacturer Postal | 97124 |
Manufacturer G1 | ACUMEDLLC |
Manufacturer Street | 5885 NE CORNELIUS PASS ROAD |
Manufacturer City | HILLSBORO OR 97124 |
Manufacturer Country | US |
Manufacturer Postal Code | 97124 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Generic Name | PROSTHESIS, ELBOW, HEMI-, RADIAL - NECK |
Product Code | KWI |
Date Received | 2020-01-28 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ACUMEDLLC |
Manufacturer Address | 5885 NE CORNELIUS PASS ROAD HILLSBORO OR 97124 US 97124 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-28 |