MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-13 for ATTUNE FEMORAL INTRODUCER 2544-01-005 254401005 manufactured by Depuy Ireland - 9616671.
[184366621]
Product complaint #: (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
[184366622]
It was reported that the screw on impactor handle broke during implantation. No surgical delay.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1818910-2020-07900 |
MDR Report Key | 9832118 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-13 |
Date of Report | 2020-02-26 |
Date of Event | 2020-02-26 |
Date Mfgr Received | 2020-02-26 |
Device Manufacturer Date | 2013-07-25 |
Date Added to Maude | 2020-03-13 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. 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 DRIVE |
Manufacturer City | WARSAW IN 465820988 |
Manufacturer Country | US |
Manufacturer Postal Code | 465820988 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ATTUNE FEMORAL INTRODUCER |
Generic Name | ATTUNE INSTRUMENTS : INSERTION DEVICES |
Product Code | HWR |
Date Received | 2020-03-13 |
Model Number | 2544-01-005 |
Catalog Number | 254401005 |
Lot Number | ABB35062 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DEPUY IRELAND - 9616671 |
Manufacturer Address | LOUGHBEG RINGASKIDDY CO. CORK EI |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-13 |