FDA Adverse Event Malfunction Summary report: N

DISPOSABLE HIP BONEC

MDR report key: 2250772 · Received September 16, 2011

Report

Report Number
1219602-2011-00153
Event Type
Malfunction
Date Received
September 16, 2011
Date of Event
August 17, 2011
Report Date
August 17, 2011
Manufacturer
SMITH & NEPHEW MANSFIELD MANUFACTURING SITE
Product Code
HAB
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

UNUSED DEVICE WAS RETURNED. INNER BLADE DOES NOT SPIN FREELY WITHIN OUTER BLADE. THE INNER BLADE WAS OBSERVED TO HAVE SOME MINOR ROUNDING OVER OF THE EDGE FORM WHICH INDICATES CONTACT WITH THE OUTER EDGE FORM. THIS IS LIKELY THE SOURCE OF THE SHEDDING. THE INNER BLADE WAS EVALUATED FOR CONFORMANCE TO DIMENSIONAL REQUIREMENTS AND WAS FOUND TO CONFORM TO DESIGN. THE OUTER BLADE WAS OBSERVED TO HAVE A TOTAL INDICATED RUNOUT IN EXCESS OF DESIGN REQUIREMENT AND FURTHER MEASUREMENT OF THE OUTER BLADE INDICATED A .004 INCH BEND AT APPROXIMATELY THE MIDDLE OF THE BLADE. THIS BEND IN THE BLADE IS LIKELY RESPONSIBLE FOR THE MISALIGNMENT OF THE INNER BLADE IN RELATION TO THE OUTER BLADE AND RESULTED IN THE METAL TO METAL CONTACT WHICH LEAD TO THE SHEDDING. (B)(4). HOWEVER, THIS PROBLEM WAS ADDRESSED (B)(4). DEVICE WAS MADE PRIOR TO THIS CHANGE TO THE PROCESS. (B)(4).

Description of Event or Problem · 1

METAL SHAVINGS - BLADE LEFT METAL SHAVING IN JOINT. ADDITIONAL INFORMATION CONFORMED THAT SURGEON IRRIGATED AS MUCH OF THE SHEDDED MATERIAL OUT AS HE COULD BUT DID NOT REMOVE ALL OF IT, THE CASE CONTINUED WITH A BACK-UP DEVICE. ORIGINAL DEVICES ARE NOT BEING RETURNED UNUSED DEVICES ARE BEING RETURNED FOR EVALUATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DISPOSABLE HIP BONEC BLADE,4.5 BONECUTTER,FR,180MM LG,DSP HAB SMITH & NEPHEW MANSFIELD MANUFACTURING SITE 7210979 50546412

Patients

Seq Age Sex Outcome Treatment
1