• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SMITH & NEPHEW, INC. 4.5MM INCISOR PLUS PLATINUM BLADE; SAW, POWERED, AND ACCESSORIES

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

SMITH & NEPHEW, INC. 4.5MM INCISOR PLUS PLATINUM BLADE; SAW, POWERED, AND ACCESSORIES Back to Search Results
Catalog Number 72203013
Device Problem Contamination /Decontamination Problem (2895)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 03/28/2019
Event Type  malfunction  
Event Description
It was reported that when using this shaver during a knee arthroscopy and debridement of the meniscus, the shaver left behind black stripes/streaks residue on the white cartilage and the meniscus.There was no significant delay or patient injuries reported but it is unknown if a backup was available to complete the procedure.No further information is available.
 
Manufacturer Narrative
One 72203013 disposable 4.5mm incisor plus platinum blade returned.The complaint stated: ¿the shaver left behind black stripes/streaks residue inner blade seemed to be stuck on initial use.¿ there were various factors that contributed to the observation.Damage being the primary catalyst.The blade is considerably bowed.This has caused skiving on the inner blade¿s outer surface where contact has been made with the outer blade.This surface condition indicates excess pressure/force was applied to the device causing the inner blade to bind with the outer.¿excessive ¿side-loading¿ on the blade during use does not improve cutting performance, and in extreme cases may result in wear and degradation of the inner blade¿.Metal shavings result from pressure during rotation.Irreversible damage may occur to blades or burrs if they are run without the flow of irrigation (dry).¿ binding and seizing can occur due to matter; tissue, bone, or metal shaving fragments not being efficiently excised.In addition, visual inspection showed blue-black tarnish of the platinum finish was present.The silver tarnish was loosened due to friction between the blade components.Remaining un-excised matter indicated less than ideal suction/irrigation to accommodate build-up of matter within the blade.The silver plating process is used to produce a device with less friction to improve performance of the device.Silicone is used for additional lubrication between inner and outer blades.Silicone and silver may is a visual observation but do not have an adverse effect on patient safety.Observations are monitored through engineering.Testing found that the results to be cosmetic.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
4.5MM INCISOR PLUS PLATINUM BLADE
Type of Device
SAW, POWERED, AND ACCESSORIES
Manufacturer (Section D)
SMITH & NEPHEW, INC.
130 forbes boulevard
mansfield MA 02048
Manufacturer (Section G)
SMITH & NEPHEW, INC.
130 forbes boulevard
mansfield MA 02048
Manufacturer Contact
jim gonzales
7000 west william cannon drive
austin, TX 78735
5123585706
MDR Report Key8491879
MDR Text Key141324311
Report Number1219602-2019-00397
Device Sequence Number1
Product Code HAB
UDI-Device Identifier03596010655660
UDI-Public03596010655660
Combination Product (y/n)N
Reporter Country CodeNZ
PMA/PMN Number
EXEMPT
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type foreign,health professional,o
Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date 04/23/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received04/08/2019
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Expiration Date09/15/2023
Device Catalogue Number72203013
Device Lot Number50759023
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer04/18/2019
Is the Reporter a Health Professional? Yes
Date Manufacturer Received04/19/2019
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured09/15/2018
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
-
-