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 2020-03-24 for ANGLED ACET INSERTR 9200-10-029 920010029 manufactured by Depuy International Ltd - 8010379.
[184752974]
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
[184752975]
The instrument? S handle has a fissure/crack. No adverse patient impact, no part broken off, no surgery surgical delay reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1818910-2020-09006 |
MDR Report Key | 9871562 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-24 |
Date of Report | 2020-03-06 |
Date of Event | 2020-03-06 |
Date Mfgr Received | 2020-03-06 |
Device Manufacturer Date | 2019-10-16 |
Date Added to Maude | 2020-03-24 |
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 | KARA DITTY-BOVARD |
Manufacturer Street | 700 ORTHOPAEDIC DR. |
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 | ANGLED ACET INSERTR |
Generic Name | HIP INSTRUMENTS : INSERTION DEVICES |
Product Code | HWR |
Date Received | 2020-03-24 |
Model Number | 9200-10-029 |
Catalog Number | 920010029 |
Lot Number | MJ3639101 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DEPUY INTERNATIONAL LTD - 8010379 |
Manufacturer Address | ST. ANTHONY'S ROAD LEEDS LS118DT UK LS11 8DT |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-24 |