MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-03-12 for ACETAB PRESSURISER 52MM(5PACK) 3206052 manufactured by Depuy Orthopaedics Inc Us.
[138915498]
If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate. Device was used for treatment, not diagnosis.
Patient Sequence No: 1, Text Type: N, H10
[138915499]
It was reported that the acetabular pressure riser (p/n: (b)(4) was broken when it was attached to t handle for cementing the acetabular side during tha surgery on (b)(6) 2019. The surgery was completed by using the spare and there was within a 30 minutes surgical delay. There were no broken parts in the patient? S body and there was no adverse consequence to the patient. No further information is available.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1818910-2019-87045 |
MDR Report Key | 8413179 |
Date Received | 2019-03-12 |
Date of Report | 2019-02-19 |
Date of Event | 2019-02-19 |
Date Mfgr Received | 2019-07-12 |
Device Manufacturer Date | 2014-04-30 |
Date Added to Maude | 2019-03-12 |
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. KARA DITTY-BOVARD |
Manufacturer Street | 1210 WARD AVENUE |
Manufacturer City | WEST CHESTER PA 193800988 |
Manufacturer Country | US |
Manufacturer Postal | 193800988 |
Manufacturer Phone | 6103142063 |
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 | 0 |
Brand Name | ACETAB PRESSURISER 52MM(5PACK) |
Generic Name | DEPUY CMW CEMENTING ACCESSORIES : CEMENT DELIVERY DEVICES |
Product Code | JDZ |
Date Received | 2019-03-12 |
Catalog Number | 3206052 |
Lot Number | 60520353 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
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 | 2019-03-12 |