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Neptune 0702014000Recalls & reported problems

Stryker Corporation · 2 Docking Station 120 V 60Hz 3A · Class 2

Adverse event reports
7
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 07613154559053), received between May 25, 2018 and Sep 25, 2020 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Electrical Shorting” (2 reports).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Electrical Shorting2
  • Melted2
  • Overheating of Device2
  • Electrical /Electronic Property Problem1
  • Fire1
  • Leak/Splash1
  • Sparking1

Patient problems

  • No Consequences Or Impact To Patient5
  • No Clinical Signs, Symptoms or Conditions2
  • Electric Shock1

Recent adverse event reports

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

  • MalfunctionSep 25, 2020Melted; Overheating of Device; Melted; Overheating of Device

    IT WAS REPORTED BY THE CUSTOMER THAT DURING TESTING OF THE DEVICE BEFORE A PROCEDURE, THE DEVICE'S PLUG WAS FOUND CHARRED. BACK-UP EQUIPMENT WAS USED TO COMPLETE THE PROCEDURE. NO CLINICALLY SIGNIFICANT DELAY, NO ADVERSE CONSEQUENCES AND NO MEDICAL INTERVENTION WERE REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10587864 ↗
  • MalfunctionSep 24, 2020Melted; Overheating of Device; Melted; Overheating of Device

    IT WAS REPORTED BY THE CUSTOMER THAT DURING TESTING OF THE DEVICE BEFORE A PROCEDURE, THE DEVICE'S PLUG WAS FOUND CHARRED. BACK-UP EQUIPMENT WAS USED TO COMPLETE THE PROCEDURE. NO CLINICALLY SIGNIFICANT DELAY, NO ADVERSE CONSEQUENCES AND NO MEDICAL INTERVENTION WERE REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10580220 ↗
  • MalfunctionJan 6, 2020Sparking; Electrical Shorting; Sparking; Electrical Shorting

    IT WAS REPORTED THAT DURING DOCKING THE DEVICE AFTER A SURGICAL PROCEDURE THE DEVICE SHORT CIRCUITED AND SPARKED. NO MEDICAL INTERVENTION AND NO ADVERSE CONSEQUENCES WERE REPORTED WITH THIS EVENT. AS THIS EVENT OCCURRED AFTER A SURGICAL PROCEDURE, THERE WAS NO PATIENT INVOLVEMENT AND NO DELAY TO A SURGICAL PROCEDURE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9553093 ↗
  • MalfunctionNov 26, 2019Electrical Shorting; Electrical Shorting

    IT WAS REPORTED THAT DURING DOCKING THE DEVICE AFTER A SURGICAL PROCEDURE AT THE USER FACILITY WATER WAS SPILLED ONTO THE RECEPTACLE CAUSING AN ELECTRICAL SHORT AND THE DEVICE TO SMOKE. NO MEDICAL INTERVENTION AND NO ADVERSE CONSEQUENCES WERE REPORTED WITH THIS EVENT. AS THIS EVENT OCCURRED AFTER A SURGICAL PROCEDURE, THERE WAS NO PATIENT INVOLVEMENT AND NO DELAY TO A SURGICAL PROCEDURE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9378998 ↗
  • MalfunctionOct 29, 2019Fire; Fire

    NO MEDICAL INTERVENTION AND NO ADVERSE CONSEQUENCES WERE REPORTED WITH THIS EVENT. AS THIS EVENT OCCURRED DURING TESTING AT THE MANUFACTURER FACILITY, THERE WAS NO PATIENT INVOLVEMENT AND NO DELAY TO A SURGICAL PROCEDURE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9251722 ↗
  • MalfunctionAug 31, 2018Leak/Splash; Leak/Splash

    IT WAS REPORTED THAT A NEPTUNE DOCKER'S HOSE WAS LEAKING AT THE USER FACILITY PRIOR TO THE START OF A SURGICAL PROCEDURE. TWO SURGICAL CASES WERE CANCELED AS A RESULT OF THE REPORTED EVENT. NO MEDICAL INTERVENTION AND NO ADVERSE CONSEQUENCES WERE REPORTED IN REGARDS TO THE EVENT. ALL CASES THAT WERE CANCELED WERE RESCHEDULED WITH NO IMPACT TO THE PATIENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7838307 ↗
  • MalfunctionMay 25, 2018Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

    IT WAS REPORTED THAT AT THE USER FACILITY A USER OF THE DEVICE RECEIVED AN ELECTRIC SHOCK AFTER THE OFF LOADING PROCESS. NO MEDICAL INTERVENTION AND NO ADVERSE CONSEQUENCES WERE REPORTED WITH THIS EVENT. AS THIS EVENT OCCURRED AFTER A PROCEDURE DURING OFF LOADING OF THE DEVICE, THERE WAS NO PATIENT INVOLVEMENT AND NO DELAY TO A SURGICAL PROCEDURE. THERE WERE NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION REQUIRED FOR THE USER OF THE DEVICE.

    Patient problems: Electric Shock; No Consequences Or Impact To Patient

    MAUDE report 7544769 ↗

Other APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED devices

All APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.