Accord 71360025Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 03596010485403), received between Feb 13, 2020 and Mar 28, 2025 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Break” (5 reports).

2 other recalls cover devices cleared under the same FDA submission (K123598); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 28, 2025Fracture; Fracture

  IT WAS REPORTED THAT DURING AN AUGMENTED HIP REPLACEMENT PROCEDURE, THE ACCORD SCISSOR CUTTER BROKE WHEN CUTTING THE CABLE. IT WAS REMOVED WITH A PAIR OF RAT-TOOTH FORCEPS. THE PROCEDURE WAS RESUMED, WITHOUT ANY DELAY, USING A S+N BACK-UP DEVICE. PATIENT WAS NOT INJURED AS CONSEQUENCE OF THIS PROBLEM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21718159 ↗
• MalfunctionOct 23, 2022Fracture; Fracture

  IT WAS REPORTED THAT, DURING SURGERY, THE ACCORD SCISSOR CUTTER BROKE WHEN THE SURGEON WAS TRYING TO CUT A CABLE OFF DURING SURGERY. IT IS UNKNOWN HOW THE PROCEDURE WAS COMPLETED AND IF THERE WAS ANY DELAY. NO PATIENT INJURIES REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15656524 ↗
• MalfunctionFeb 7, 2022Break; Break

  IT WAS REPORTED THAT AN ACCORD SCISSOR CUTTER WAS FOUND TO BE BROKEN, ONE OF THE TIPS BROKE OFF COMPLETELY. AS THIS WAS NOTICED UPON INSPECTION, THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13470383 ↗
• MalfunctionNov 23, 2021Break; Break

  IT WAS REPORTED THAT A ACCORD SCISSOR CUTTER IS BROKEN. AS THIS WAS NOTICED UPON FIELD INSPECTION, THERE WAS NOT PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12866127 ↗
• MalfunctionSep 27, 2021Break; Break

  IT WAS REPORTED THAT AN ACCORD SCISSOR CUTTER BROKE. AS THIS WAS NOTICED UPON CLEANING AND STERILIZATION ACTIVITIES, THERE WAS NOT PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12538196 ↗
• MalfunctionJul 12, 2021Break; Break

  IT WAS REPORTED THAT AN ACCORD SCISSOR CUTTER WAS FOUND BROKEN DURING STERILIZATION PROCESS. AS THIS WAS NOTICED IN A NON-SURGICAL ENVIRONMENT, THERE WAS NOT ANY PATIENT INVOLVED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12151218 ↗
• MalfunctionFeb 13, 2020Break; Break

  IT WAS REPORTED THAT DURING SURGERY, ACCORD SCISSOR CUTTING MECHANISM BROKE WHILE BEING USED. NO DELAY. NO CONFIRMATION OF A BACKUP DEVICE RECEIVED. NO IMPACT OR INJURY TO PATIENT REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9705912 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K123598. One submission often covers many models, so check the product and lot details in each record.

• Z-0730-2019 · Jan 7, 2019 · Terminated
  SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM, S&N 75004613
• Z-1008-2017 · Nov 16, 2016 · Terminated
  REFLECTION(R) DEAD BLOW MALLET, REF 71362106, QTY: (1), NON-STERILE, Smith & Nephew, Inc,. Memphis, TN 38116