inforMED
MalfunctionLRO

SMALL GENERAL PACK

Received Dec 5, 2025 · Event occurred Oct 1, 2025

Report 3005011024-2025-00015 · MDR key 23726708

Device

Generic name

General Surgery Tray

Model number

89-2580

Lot number

62457410

Product problems

  • Component Missing
  • Component Missing

Patient

NA · Unknown

  • No Clinical Signs, Symptoms or Conditions
  • No Clinical Signs, Symptoms or Conditions

Narrative

Description of Event or Problem

A USER FACILITY REPORTED THROUGH A MEDWATCH, "THERE WAS NOT RULER IN THE PACK."

Additional Manufacturer Narrative

A USER FACILITY REPORTED VIA A MEDWATCH, "THERE WAS NOT RULER IN THE PACK. " DEROYAL INDUSTRIES, INC. REQUESTED RETURN OF THE DEVICE, BUT IT WAS LISTED AS NOT AVAILABLE FOR RETURN. DEROYAL REVIEWED THE WORK ORDER FOR THE LOT REPORTED WITH THE COMPLAINT AND DID NOT FIND ANY ISSUES. EMPLOYEES SIGNED OFF ON ADDING THE RULER TO THE PACK AS SPECIFIED. INVENTORY WAS NOT ABLE TO BE CHECKED AS NO INVENTORY WAS AVAILABLE AT DISTRIBUTION AND NO FURTHER INVENTORY IS BEING CREATED AS THE MANUFACTURING SITE HAS CLOSED. THE RISK ANALYSIS WAS REVIEWED AND WAS FOUND TO BE UP-TO-DATE AND DID NOT REQUIRE ANY UPDATES. A COMPLAINT TO SALES RATIO WAS CONDUCTED FOR OVER THE PAST TWO YEARS AND FOUND TO BE 0.011%. ROOT CAUSE: THE EXACT ROOT CAUSE WAS UNABLE TO BE DETERMINED AS NO ISSUES WERE DISCOVERED IN THE PRODUCTION RECORDS AND WITHOUT A RETURNED PRODUCT AND NO FURTHER INVENTORY BEING PRODUCED, NO FURTHER INFORMATION COULD BE GATHERED. CORRECTIVE AND PREVENTIVE ACTIONS: BECAUSE THE ROOT CAUSE WAS UNABLE TO BE DETERMINED AND BECAUSE THE MANUFACTURING SITE OF THE DEVICE, LAFOLLETTE, HAS CLOSED, NO CORRECTIVE OR PREVENTIVE ACTIONS WILL BE TAKEN. THERE IS NO OTHER ADDITIONAL INFORMATION AVAILABLE AS THE MANUFACTURING SITE OF THIS PRODUCT IN LAFOLLETTE, TENNESSEE HAS BEEN CLOSED. THIS INVESTIGATION IS COMPLETE AT THIS TIME. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME. WE WILL PROVIDE A FOLLOW-UP REPORT IF ADDITIONAL INFORMATION BECOMES AVAILABLE.