inforMED
MalfunctionLRZ

STRAIGHT SCREWDRIVER

Received Aug 28, 2020 · Event occurred Aug 4, 2020

Report 1020279-2020-04286 · MDR key 10469243

Device

Generic name

Screwdriver, Surgical

Model number

71362293

Catalog number

71362293

Lot number

09DM06909

Product problems

  • Material Deformation
  • Material Deformation

Patient

Not reported

  • No Known Impact Or Consequence To Patient
  • No Known Impact Or Consequence To Patient

Narrative

Additional Manufacturer Narrative

THE DEVICE, INTENDED FOR USE IN TREATMENT, WAS RETURNED FOR EVALUATION A VISUAL INSPECTION CONFIRMS THE STRAIGHT SCREWDRIVER IS STRIPPED AND ROUNDED OFF ON BOTH ENDS OF THE DEVICE. THE DEVICE SHOWS EXTENSIVE SIGNS OF WEAR/USAGE. THE DEVICE WAS MANUFACTURED IN 2009. A REVIEW OF COMPLAINT HISTORY ON THE LISTED PART REVEALED NO PRIOR COMPLAINTS FOR THE LISTED BATCH WITH THE SAME FAILURE MODE. A REVIEW OF THE MANUFACTURING RECORDS DID NOT REVEAL A MANUFACTURING ABNORMALITY THAT COULD HAVE CAUSED OR CONTRIBUTED TO THE REPORTED INCIDENT. 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 COMPLAINTS WILL BE REOPENED. NO FURTHER INVESTIGATION IS WARRANTED FOR THESE COMPLAINTS; HOWEVER WE WILL CONTINUE TO MONITOR FOR FUTURE COMPLAINTS AND INVESTIGATE AS NECESSARY. WE CONSIDER THIS INVESTIGATION CLOSED.

Description of Event or Problem

IT WAS REPORTED THAT THE END OF DRIVER WAS FOUND ROUNDED DURING SET UP OR INSPECTION. NO DELAY OR INJURY REPORTED.