FDA Adverse Event Malfunction Summary report: N

RECON ULNAR STEM IMPLANT #3, 20MM EXTENSION

MDR report key: 5319938 · Received December 22, 2015

Report

Report Number
0008031020-2015-00603
Event Type
Malfunction
Date Received
December 22, 2015
Date of Event
July 17, 2013
Report Date
July 17, 2013
Manufacturer
STRYKER GMBH
Product Code
KXE
PMA / PMN Number
K010786-LTF
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

WITH GUIDANCE FROM THE MDR POLICY BRANCH OF THE FDA, MDR REPORTED BY STRYKER (B)(4) AS A RESULT OF A RETROSPECTIVE LOOKBACK OF COMPLAINTS RESULTING FROM THE ACQUISITION OF ASSETS FROM (B)(4). DEVICE WILL NOT BE RETURNED. IF ADDITIONAL INFORMATION BECOMES AVAILABLE IT WILL BE PROVIDED ON A SUPPLEMENTAL REPORT. THE REPORTED DEVICE WAS MANUFACTURED AND DISTRIBUTED BY (B)(4) AND IMPLANTED PRIOR TO HOWMEDICA OSTEONICS CORP.¿S PURCHASE OF CERTAIN ASSETS OF (B)(4) ON AUGUST 1, 2014. STRYKER BECAME LEGAL MANUFACTURER OF THIS PRODUCT ON APRIL 1, 2015 AND HAS TAKEN THE RESPONSIBILITY FOR MEDICAL DEVICE REPORTING. DEVICE IS NOT AVAILABLE TO STRYKER.

Description of Event or Problem · 1

IMPLANT BREAKING THROUGH PACKAGING (RNC 3425) - (B)(4) IS CURRENTLY CONDUCTING A RECOVERY OF PACKAGED PRODUCT ASSOCIATED WITH THE PACKAGING BREACH. THIS ACTIVITY WILL REPACKAGE (B)(4) PRODUCT WITH A (2) YEAR EXPIRATION DATE. CONCURRENTLY A NEW PACKAGE DESIGN IS UNDER VALIDATION

Description of Event or Problem · 1

IMPLANT BREAKING THROUGH PACKAGING ((B)(4)) - SBI IS CURRENTLY CONDUCTING A RECOVERY OF PACKAGED PRODUCT ASSOCIATED WITH THE PACKAGING BREACH. THIS ACTIVITY WILL REPACKAGE SBI PRODUCT WITH A (2) YEAR EXPIRATION DATE. CONCURRENTLY A NEW PACKAGE DESIGN IS UNDER VALIDATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
845358 RECON ULNAR STEM IMPLANT #3, 20MM EXTENSION PROSTHESIS, WRIST, HEMI-, ULNAR KXE STRYKER GMBH 12214

Patients

Seq Age Sex Outcome Treatment
1 Other