TAPER SLEEVE ADAPTER 12/14 +2
Report
- Report Number
- 1818910-2013-21942
- Event Type
- Injury
- Date Received
- July 23, 2013
- Date of Event
- November 9, 2012
- Report Date
- April 29, 2015
- Manufacturer
- DEPUY INTL., LTD. - 8010379
- Product Code
- JDI
- Removal / Correction Number
- Z-1749/1816-2011
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- PATIENT
Narratives
NO 510(K) NUMBER PROVIDED BECAUSE THIS IMPLANT IS SOLD INTERNATIONALLY WITH DIFFERENT INDICATIONS FOR USE; IT IS CURRENTLY SOLD IN THE US UNDER A DIFFERENT PART NUMBER. THE ASR PLATFORM WAS VOLUNTARILY RECALLED FROM THE MARKET IN AUGUST 2010, AND THE ASR PRODUCT CODES ARE NOW CONSIDERED INACTIVE. FURTHER INVESTIGATION OF THIS INDIVIDUAL INCIDENT WILL NOT BE UNDERTAKEN, AS THERE IS AN ONGOING INVESTIGATION REGARDING THE ROOT CAUSE(S) AND/OR CORRECTIVE ACTIONS. (B)(4). DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT AND/OR ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED.
DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED. SHOULD ADDITIONAL INFORMATION BE RECEIVED THE INVESTIGATION WILL BE REOPENED.
DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED.
REASON(S) FOR REVISION: UNKNOWN.
UPDATE: APRIL 19, 2017. REASONS FOR REVISION: PAIN / ALVAL /SOFT TISSUE REACTION.
UPDATE 29 APR 2015: REC'D CRAWFORDS CLAIMSUITE, SURGEON, ADDITIONAL HOSPITAL - (B)(6), FILE HANDLER, MW FIELDS, MANUFACTURING DATE AND LOCATION, EXPIRY DATES FOR ALL PRODUCTS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 342276 | TAPER SLEEVE ADAPTER 12/14 +2 | HIP FEMORAL STEM/SLEEVE | JDI | DEPUY INTL., LTD. - 8010379 | 1850838 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |