FMS 282114Recalls & reported problems

Summary

The FDA's MAUDE database contains 123 adverse event reports that list this exact device (DI 10886705020485), received between Jan 12, 2018 and Apr 27, 2026 — classified as 2 injuries, 121 malfunctions.

The most frequently reported specific device problem is “Infusion or Flow Problem” (73 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

Recent adverse event reports

The 25 most recent of 123 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 27, 2026Output Problem

  IT WAS REPORTED THAT DURING AN UNSPECIFIED PROCEDURE, TWO FMS INTERFACE CABLES WERE BROKEN AND MALFUNCTIONING. THIS IS REPORT 1 OF 2 FOR (B)(4). THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2026.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25002049 ↗
• MalfunctionApr 21, 2026Use of Device Problem; Infusion or Flow Problem

  IT WAS REPORTED THAT THE FMS CONNECT DEVICE WAS DAMAGED. IT WAS NOT REPORTED IF THE DEVICE WAS USED IN A SURGICAL PROCEDURE. DURING IN-HOUSE ENGINEERING EVALUATION IT WAS DETERMINED THAT THE SUCTION OF THE DEVICE COULD NOT BE ACTIVATED. THERE WAS NO CONSEQUENCE OR IMPACT TO THE PATIENT, AND NO SIGNS, SYMPTOMS, OR PATIENT INVOLVEMENT WERE IDENTIFIED. THE EXACT DATE OF THE EVENT WAS NOT REPORTED; HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2026. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24937324 ↗
• MalfunctionApr 11, 2026Use of Device Problem; Infusion or Flow Problem

  IT WAS REPORTED THAT DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD A SUCTION FAILURE. IT WAS INITIALLY REPORTED THAT THREE FMS CONNECT INTERFACE CABLE VUE DEVICES WERE NOT WORKING. IT WAS NOT REPORTED IF THE DEVICE WAS USED IN SURGERY. IT WAS NOT REPORTED IF THERE WERE ANY DELAYS IN A SURGICAL PROCEDURE OR IF A SPARE DEVICE WAS AVAILABLE. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2026. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24846094 ↗
• MalfunctionApr 11, 2026Use of Device Problem; Infusion or Flow Problem

  IT WAS REPORTED THAT DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD A SUCTION FAILURE. IT WAS INITIALLY REPORTED THAT THREE FMS CONNECT INTERFACE CABLE VUE DEVICES WERE NOT WORKING. IT WAS NOT REPORTED IF THE DEVICE WAS USED IN SURGERY. IT WAS NOT REPORTED IF THERE WERE ANY DELAYS IN A SURGICAL PROCEDURE OR IF A SPARE DEVICE WAS AVAILABLE. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2026. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24845923 ↗
• MalfunctionApr 10, 2026Use of Device Problem; Infusion or Flow Problem

  IT WAS REPORTED THAT DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD A SUCTION FAILURE. IT WAS INITIALLY REPORTED THAT THREE FMS CONNECT INTERFACE CABLE VUE DEVICES WERE NOT WORKING. IT WAS NOT REPORTED IF THE DEVICE WAS USED IN SURGERY. IT WAS NOT REPORTED IF THERE WERE ANY DELAYS IN A SURGICAL PROCEDURE OR IF A SPARE DEVICE WAS AVAILABLE. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2026. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24845859 ↗
• MalfunctionMar 26, 2026Output Problem

  IT WAS REPORTED THAT THE FMS CONNECT (VUE) DEVICE SHOWED MULTIPLE ERROR CODES THROUGHOUT SURGERY. DEVICE ACTIVATES OUTFLOW WHEN "RF" IS ACTIVATED IN ADDITION TO THE SHAVER. DEVICE MAKES CLICKING SOUNDS PRIOR TO ANYTHING ATTACHED AND CONTINUES CLICKS THROUGHOUT PROCEDURE, EVEN IF APPEARS AS OPERATING CORRECTLY. DEVICE RANDOMLY BEEPS AND STOPS / RESTARTS. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2026. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24699792 ↗
• MalfunctionMar 23, 2026Infusion or Flow Problem; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED THAT CABLE OF THE FMS CONNECT (VUE) DEVICE WAS MALFUNCTIONING. DURING IN-HOUSE ENGINEERING EVALUATION, A TEST SHAVER HANDPIECE WAS WIRED THROUGH THE INTERFACE CABLE, AND WHEN THE SHAVER WAS ACTIVATED, THE BLUE INDICATOR LIGHT WAS FLASHING ON THE DEVICE INDICATING THE INTERFACE CABLE DID RECOGNIZE THE CURRENT GOING THROUGH THE TEST SHAVER, HOWEVER THE PINCH VALVE ON THE PUMP WAS NOT ACTIVATING. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION, OR PROLONGED HOSPITALIZATION. THE EXACT DATE OF THE EVENT WAS NOT REPORTED; HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2026. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24662237 ↗
• MalfunctionMar 18, 2026Blocked Connection; Infusion or Flow Problem

  IT WAS REPORTED THAT DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD A SUCTION FAILURE. IT WAS INITIALLY REPORTED THAT DURING A SHOULDER ARTHROSCOPY SURGICAL PROCEDURE, IT WAS DISCOVERED THAT THREE SEPARATE DEVICES WERE READING AS SHAVER AND NOT AS INTERFACE CABLE. IT WAS REPORTED THAT THE DEVICES WERE USED WITH THE FMS VUE, HEALIX ADVANCE, AND MUSTANG DEVICES AND DID NOT CONTRIBUTE TO THE REPORTED EVENT. THERE WERE NO DELAYS TO THE SURGICAL PROCEDURE. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24634845 ↗
• MalfunctionMar 18, 2026Blocked Connection; Infusion or Flow Problem

  IT WAS REPORTED THAT DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD A SUCTION FAILURE. IT WAS INITIALLY REPORTED THAT DURING A SHOULDER ARTHROSCOPY SURGICAL PROCEDURE, IT WAS DISCOVERED THAT THREE SEPARATE DEVICES WERE READING AS SHAVER AND NOT AS INTERFACE CABLE. IT WAS REPORTED THAT THE DEVICES WERE USED WITH THE FMS VUE, HEALIX ADVANCE, AND MUSTANG DEVICES AND DID NOT CONTRIBUTE TO THE REPORTED EVENT. THERE WERE NO DELAYS TO THE SURGICAL PROCEDURE. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24634361 ↗
• MalfunctionMar 18, 2026Blocked Connection; Infusion or Flow Problem

  IT WAS REPORTED THAT DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD A SUCTION FAILURE. IT WAS INITIALLY REPORTED THAT DURING A SHOULDER ARTHROSCOPY SURGICAL PROCEDURE, IT WAS DISCOVERED THAT THREE SEPARATE DEVICES WERE READING AS SHAVER AND NOT AS INTERFACE CABLE. IT WAS REPORTED THAT THE DEVICES WERE USED WITH THE FMS VUE, HEALIX ADVANCE, AND MUSTANG DEVICES AND DID NOT CONTRIBUTE TO THE REPORTED EVENT. THERE WERE NO DELAYS TO THE SURGICAL PROCEDURE. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24630676 ↗
• MalfunctionMar 18, 2026Output Problem

  IT WAS REPORTED THAT DURING AN UNSPECIFIED PROCEDURE, THE FMS CONNECT (VUE) SHOWED MULTIPLE ERROR CODES THROUGHOUT CASE. THE DEVICE ACTIVATED THE OUTFLOW WHEN IT WAS ACTIVATED IN ADDITION TO THE SHAVER. THE DEVICE MADE CLICKING SOUNDS PRIOR TO ANYTHING ATTACHED AND CONTINUED CLICKS THROUGHOUT THE PROCEDURE, EVEN IF IT APPEARED TO BE OPERATING CORRECTLY. THE DEVICE RANDOMLY BEEPED, STOPPED AND RESTARTED. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2026.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24627538 ↗
• MalfunctionMar 17, 2026Blocked Connection; Infusion or Flow Problem; Output Problem

  IT WAS REPORTED THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE IT WAS OBSERVED THAT THERE WAS AN ERROR WITH THE FMS CONNECT (VUE) INTERFACE CABLE DEVICE AS THE DEVICE WAS NOT RESPONDING TO THE SHAVER DEVICE RUNNING AS IT SHOULD. IT WAS REPORTED THAT ALTERNATIVE ADAPTERS WERE USED TO COMPLETE THE PROCEDURE. DURING IN-HOUSE ENGINEERING EVALUATION IT WAS DETERMINED THAT WHEN A TEST SHAVER HANDPIECE WAS WIRED THROUGH THE INTERFACE CABLE AND ACTIVATED, THE BLUE INDICATOR LIGHT WAS FLASHING ON THE DEVICE INDICATING THE INTERFACE CABLE DID RECOGNIZE THE CURRENT GOING THROUGH THE TEST SHAVER, HOWEVER THE PINCH VALVE ON THE PUMP WAS NOT ACTIVATING. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT. NO ADDITIONAL INFORMATION COULD BE PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24616195 ↗
• MalfunctionFeb 25, 2026Use of Device Problem; Blocked Connection

  IT WAS REPORTED BY SALES REP VIA PHONE THAT DURING AN UNKNOWN ARTHROSCOPIC PROCEDURE, THE FMS CONNECT (VUE) DEVICE CABLE WAS NOT PROPERLY SYNCING THE SHAVER BOX WITH THE FMS DEVICE DESPITE MULTIPLE ATTEMPTS. IT IS NOT FUNCTIONING. ANOTHER DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO DELAY IN THE PROCEDURE REPORTED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24447901 ↗
• MalfunctionFeb 13, 2026Use of Device Problem; Suction Failure

  IT WAS REPORTED THAT DURING EVALUATION, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD A SUCTION FAILURE. IT WAS NOTED IN THE SERVICE ORDER THAT THE DEVICE HAD A BROKEN INTERFACE CABLE AND WAS NO LONGER FUNCTIONING. THIS EVENT DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT INVOLVEMENT. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION, OR PROLONGED HOSPITALIZATION. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2026. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24337362 ↗
• MalfunctionFeb 13, 2026Use of Device Problem; Suction Failure

  IT WAS REPORTED THAT DURING EVALUATION, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD A SUCTION FAILURE. IT WAS NOTED IN THE SERVICE ORDER THAT THE DEVICE HAD A BROKEN INTERFACE CABLE AND WAS NO LONGER FUNCTIONING. THIS EVENT DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT INVOLVEMENT. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION, OR PROLONGED HOSPITALIZATION. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2026. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24337086 ↗
• MalfunctionJan 29, 2026Use of Device Problem

  IT WAS REPORTED THAT DURING SERVICE AND EVALUATION, IT WAS DETERMINED THAT THE FMS CONNECT DEVICE HAD SUCTION FAILURE. IT WAS REPORTED IN THE SERVICE ORDER THAT THE DEVICE INTERFACE HAD AN UNKNOWN ISSUE. IT WAS UNKNOWN WHEN THE EVENT OCCURRED. THERE WERE NO REPORTS OF DELAYS TO A SURGICAL PROCEDURE. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. THE DATE OF EVENT WAS UNKNOWN BUT WAS KNOWN TO HAVE OCCURRED IN 2025. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24215259 ↗
• MalfunctionJan 23, 2026Use of Device Problem; Suction Failure

  IT WAS REPORTED THAT DURING EVALUATION OF THE DEVICE, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD SUCTION FAILURE. IT WAS INITIALLY REPORTED THAT THE DEVICE HAD UNKNOWN ISSUE. THIS EVENT DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT INVOLVEMENT. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION, OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2025.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24164009 ↗
• MalfunctionJan 16, 2026Appropriate Device Problem Term/Code Not Available; Suction Failure

  IT WAS REPORTED THAT DURING EVALUATION OF THE DEVICE, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD SUCTION FAILURE. IT WAS REPORTED INITIALLY THAT THE DEVICE HAD AN UNSPECIFIED MALFUNCTION. THIS EVENT DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT INVOLVEMENT. THE EXACT DATE OF THIS EVENT WAS UNKNOWN BUT WAS NOTED TO HAVE OCCURRED IN 2025. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION, OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24100560 ↗
• MalfunctionJan 15, 2026Use of Device Problem

  IT WAS REPORTED THAT DURING SERVICE AND EVALUATION, IT WAS DETERMINED THAT THE FMS CONNECT DEVICE SUCTION FAILED. IT WAS REPORTED IN THE SERVICE ORDER THAT THE DEVICE INTERFACE CABLE FAILED AND WAS NOT FUNCTIONING. IT WAS UNKNOWN WHEN THE EVENT OCCURRED. THERE WERE NO REPORTS OF DELAYS TO A SURGICAL PROCEDURE. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. THE DATE OF EVENT WAS UNKNOWN BUT WAS KNOWN TO HAVE OCCURRED IN 2025. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24079251 ↗
• MalfunctionDec 29, 2025Blocked Connection; Infusion or Flow Problem; Blocked Connection; Infusion or Flow Problem

  IT WAS REPORTED THAT PRIOR TO A SURGICAL PROCEDURE IT WAS OBSERVED THAT THE FMS CONNECT (VUE) DEVICE WAS NOT READING PROPERLY THUS DID NOT CREATE SUCTION WHEN USING THE SHAVER. THERE WAS NO DELAY IN THE PROCEDURE REPORTED. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23911265 ↗
• MalfunctionDec 15, 2025Blocked Connection; Infusion or Flow Problem; Blocked Connection; Infusion or Flow Problem

  REPORT 2 OF 2 FOR (B)(4). IT WAS REPORTED THAT DURING AN UNKNOWN SURGERY, WHILE USING THE FMS VUE PUMP DEVICE AND FMS CONNECT (VUE) DEVICE, IT WAS OBSERVED THAT THE PUMP GAVE MULTIPLE ERRORS CODES AND IT INCORRECTLY RECOGNIZED THE INTERFACE CABLE AS A SHAVER. DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE DEVICE HAD SUCTION FAILURE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23806198 ↗
• MalfunctionDec 9, 2025Use of Device Problem; Suction Failure; Use of Device Problem; Suction Failure

  IT WAS REPORTED THAT DURING EVALUATION OF THE DEVICE, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD A SUCTION FAILURE. IT WAS INITIALLY REPORTED THAT THE DEVICE WAS NOT FUNCTIONING PROPERLY. THIS EVENT DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT INVOLVEMENT. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION, OR PROLONGED HOSPITALIZATION. THE EXACT DATE OF THIS EVENT IS UNKNOWN. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23760056 ↗
• MalfunctionDec 5, 2025Use of Device Problem; Infusion or Flow Problem; Use of Device Problem; Infusion or Flow Problem

  IT WAS REPORTED THAT DURING EVALUATION OF THE DEVICE, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD A SUCTION FAILURE. IT WAS INITIALLY REPORTED THAT THE DEVICE CABLE WAS BROKEN AND NOT FUNCTIONING. THIS EVENT DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT INVOLVEMENT. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION, OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23726330 ↗
• MalfunctionDec 4, 2025Blocked Connection; Infusion or Flow Problem; Blocked Connection; Infusion or Flow Problem

  IT WAS REPORTED THAT DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD A SUCTION FAILURE. IT WAS INITIALLY REPORTED THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE, IT WAS DISCOVERED THAT THE DEVICE PUMP GAVE MULTIPLE UNRECOGNIZABLE ERRORS CODES, AND IT WAS INCORRECTLY RECOGNIZING THE INTERFACE CABLE AS A SHAVER DEVICE. IT WAS NOT REPORTED IF THERE WERE ANY DELAYS TO THE SURGICAL PROCEDURE OR IF A SPARE DEVICE WAS AVAILABLE FOR USE. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2025. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23722987 ↗
• MalfunctionDec 4, 2025Blocked Connection; Infusion or Flow Problem; Blocked Connection; Infusion or Flow Problem

  IT WAS REPORTED THAT DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE FMS CONNECT (VUE) DEVICE HAD A SUCTION FAILURE. IT WAS INITIALLY REPORTED THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE, IT WAS DISCOVERED THAT THE DEVICE PUMP GAVE MULTIPLE UNRECOGNIZABLE ERRORS CODES, AND IT WAS INCORRECTLY RECOGNIZING THE INTERFACE CABLE AS A SHAVER DEVICE. IT WAS NOT REPORTED IF THERE WERE ANY DELAYS TO THE SURGICAL PROCEDURE OR IF A SPARE DEVICE WAS AVAILABLE FOR USE. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2025. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23722943 ↗