FDA Adverse Event Injury Summary report: N

TAPER SLEEVE ADAPTER 12/14 +2

MDR report key: 3243746 · Received July 23, 2013

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

Additional Manufacturer Narrative · 1

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.

Additional Manufacturer Narrative · 1

DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED. SHOULD ADDITIONAL INFORMATION BE RECEIVED THE INVESTIGATION WILL BE REOPENED.

Additional Manufacturer Narrative · 1

DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED.

Description of Event or Problem · 1

REASON(S) FOR REVISION: UNKNOWN.

Description of Event or Problem · 1

UPDATE: APRIL 19, 2017. REASONS FOR REVISION: PAIN / ALVAL /SOFT TISSUE REACTION.

Description of Event or Problem · 1

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