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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SMITH & NEPHEW, INC. META-TAN LAG SCREW DRIVER; ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

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SMITH & NEPHEW, INC. META-TAN LAG SCREW DRIVER; ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES Back to Search Results
Model Number 71631440
Device Problem Material Deformation (2976)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 02/24/2021
Event Type  Injury  
Manufacturer Narrative
(b)(4).
 
Event Description
It was reported that during surgery of meta tan nail removal, the mating part on the lag screw broke ((b)(4)).Meta-tan lag screw driver inner rod bent and outer rod deformed ((b)(4)).Then, they tried to continue using lag screw driver, inner rod bent and outer rod deformed ((b)(4)).Then the surgeon drilled bone around the lag screw drilled and tried to removing a lag screw with a pench.The lag screw could not removed.They gave up removing the lag screw and the nail.3 hours surgical delay.
 
Manufacturer Narrative
The device, used in treatment, was returned for evaluation.A visual inspections of the returned device confirms the lag screw driver is deformed and the lag screw rod is bent.The device exhibits signs of significant wear and use.A review of complaint history did not reveal additional complaints for the listed batch.A review of the manufacturing records did not reveal a manufacturing abnormality that could have caused or contributed to the reported incident.A review of the risk management file revealed this failure mode was previously identified.This device is a reusable instrument that can be exposed to numerous surgeries; damage from repeated use can occur.Expected wear/tear is likely the probable cause of the reported event.We recommend that all reusable instruments be routinely inspected for wear and damage and replaced as necessary.At this time, we have no reason to suspect that the product failed to meet any product specifications at the time of manufacture.Based on this investigation, the need for corrective action is not indicated.Should additional information be received, the complaint will be reopened.No further investigation warranted for this complaint; however we will continue to monitor for future complaints and investigate as necessary.We consider this investigation closed.
 
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Brand Name
META-TAN LAG SCREW DRIVER
Type of Device
ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES
Manufacturer (Section D)
SMITH & NEPHEW, INC.
1450 brooks rd.
memphis TN 38116
MDR Report Key11510080
MDR Text Key240639426
Report Number1020279-2021-02210
Device Sequence Number1
Product Code HSB
UDI-Device Identifier00885556158340
UDI-Public00885556158340
Combination Product (y/n)N
PMA/PMN Number
K122170
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,foreig
Type of Report Initial,Followup
Report Date 06/23/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/17/2021
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number71631440
Device Catalogue Number71631440
Device Lot Number20CSP0003
Was Device Available for Evaluation? No
Date Manufacturer Received06/18/2021
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
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