Paradigm® REAL-Time Revel™ MMT-723RNAS (UDI 00643169476677)Recalls & reported problems

Summary

The FDA's MAUDE database contains 258 adverse event reports that list this exact device (DI 00643169476677), received between May 26, 2017 and Jul 22, 2020 — classified as 4 deaths, 101 injuries, 153 malfunctions.

The most frequently reported specific device problem is “Device Difficult to Program or Calibrate” (41 reports).

14 other recalls cover devices cleared under the same FDA submission (P980022); 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 18, 2026.

Most reported problems

Recent adverse event reports

The 25 most recent of 258 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 22, 2020Mechanical Problem; Obstruction of Flow; Battery Problem; Moisture or Humidity Problem; Patient Device Interaction Problem; Mechanical Problem; Obstruction of Flow; Battery Problem; Moisture or Humidity Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD SCRATCHES AND THAT HARD TO READ. CUSTOMER ALSO SAID HE EXPERIENCED SLOW REWOUND, BATTERY LAST LESS THAN EXPECTED, AND RANDOM NO DELIVERY ALARM. CUSTOMER ALSO STATED THAT INSULIN PUMP HAD INSULIN FLOW BLOCK ALARM AND IT WAS RESOLVED BY COMPLETE SET CHANGE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10306679 ↗
• MalfunctionJul 16, 2020Mechanical Problem; Battery Problem; Patient Device Interaction Problem; Mechanical Problem; Battery Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP RECEIVED MOTOR ERROR ALARM. INSULIN PUMP RECEIVED NO DELIVERY ALARMS FREQUENTLY. CUSTOMER WAS DECLINED TROUBLESHOOTING. CUSTOMER ALSO HAD SOME BATTERY ISSUES. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10281499 ↗
• MalfunctionJul 6, 2020Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP BUTTONS WERE NOT RESPONDING. CUSTOMER STATED THEY WERE UNABLE TO CLEAR THE ALARM AND ALSO TIME WAS ADVANCED. TROUBLESHOOTING WAS PERFORMED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10231659 ↗
• DeathJun 24, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED VIA PHONE CALL THAT THE CUSTOMER PASSED AWAY AT HOME. THE CUSTOMER WAS HOSPITALIZED ON (B)(6) 2020 AND THEN THEY WERE DISCHARGED. THE CAUSE OF DEATH WAS BELIEVED TO BE A MASSIVE STROKE RELATED TO HEART PROBLEMS. THE CALLER STATED THAT THE CUSTOMER HAD HEART PROBLEMS AND STROKES THAT MAY HAVE LED TO THE CUSTOMER'S PASSING. THE CUSTOMER¿S BLOOD GLUCOSE WAS OVER 500 MG/DL AT THE TIME OF ADMISSION. THE CUSTOMER WAS NOT WEARING THE INSULIN PUMP AT THE TIME OF DEATH. THE INSULIN PUMP HAD BEEN DISCONNECTED MORE THAN 48 HOURS PRIOR TO PASSING. THE CUSTOMER WAS USING MANUAL INJECTIONS AFTER THEY GOT DISCHARGED. THE CUSTOMER WAS NOT USING SENSORS. THE CALLER DECLINED TO RETURN THE INSULIN PUMP FOR ANALYSIS.

  Patient problems: Death; Hyperglycemia

  MAUDE report 10187403 ↗
• MalfunctionJun 2, 2020Obstruction of Flow; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD NO DELIVERY ALARM. CUSTOMER STATED THEY HAD TRIED ALL REMEDIES. TROUBLESHOOTING WAS PERFORMED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WIL BE RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

  MAUDE report 10107574 ↗
• MalfunctionJun 1, 2020Obstruction of Flow; Obstruction of Flow

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY RECEIVED A NO DELIVERY ALARM. THE USER STATED THE NO DELIVERY ALARM OCCURRED PREVIOUS TIMES AND HAS CALLED TO REPORT TO MEDTRONIC. BLOOD GLUCOSE LEVEL AT THE TIME OF THE INCIDENT WAS UNKNOWN. TROUBLESHOOTING WAS COMPLETED FOR THE NO DELIVERY ALARM. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10104478 ↗
• MalfunctionJun 1, 2020Excess Flow or Over-Infusion; Insufficient Flow or Under Infusion; Power Problem; Excess Flow or Over-Infusion; Insufficient Flow or Under Infusion; Power Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP WAS NOT DELIVERING THE CORRECT AMOUNTS OF INSULIN. THE CUSTOMER STATED THEY WERE HAVING UNEXPLAINED HIGHS AND ALMOST RECEIVED EMERGENCY MEDICAL ASSISTANCE, BUT WAS ABLE TO STABILIZE THEIR BLOOD GLUCOSE LEVELS. THE CUSTOMER ALSO MENTIONED THE PUMP REJECTS NEW BATTERIES. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. TROUBLESHOOTING WAS NOT COMPLETED AS THE CUSTOMER DECLINED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 10104467 ↗
• MalfunctionMay 12, 2020Premature Discharge of Battery; Premature Discharge of Battery

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP RECEIVED UNEXPECTED ALARM. CUSTOMER REPORTED THAT THEY WERE ABLE TO CLEAR THE ALARM AND ABLE TO REWIND THE INSULIN PUMP. CUSTOMER REPORTED THAT THE INSULIN PUMP DID EXPERIENCED UNEXPECTED RESTART. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10046064 ↗
• MalfunctionMay 6, 2020No Display/Image; Device Difficult to Program or Calibrate; Moisture or Humidity Problem; Patient Device Interaction Problem; No Display/Image; Device Difficult to Program or Calibrate; Moisture or Humidity Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE CUSTOMER WENT FOR SWIMMING AND NOW INSULIN PUMP WON'T WORK. THE CUSTOMER STATED THAT THE INSULIN PUMP HAD BUTTON ERROR. THE CUSTOMER ALSO STATED THAT THE MINUTES ARE ADVANCING. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10028416 ↗
• MalfunctionMar 26, 2020Mechanical Problem; Obstruction of Flow; Mechanical Problem; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP RECEIVED MULTIPLE MOTOR ERRORS AND NO DELIVERY ALARM. THE CUSTOMER ALSO REPORTED THAT THEY WERE ABLE TO CLEAR THE ALARM. THE CUSTOMER WAS ABLE TO COMPLETE INSULIN PUMP REWIND. THE CUSTOMER REPORTED THAT THE DRIVE SUPPORT CAP WAS NORMAL. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9887225 ↗
• MalfunctionMar 18, 2020Device Difficult to Program or Calibrate; Patient Device Interaction Problem; Device Difficult to Program or Calibrate; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP'S BUTTONS HAD TO PRESS TWICE. THE CUSTOMER STATED THERE WAS CRACKS IN CASING NEAR BATTERY CAP. CUSTOMER DECLINED TO TROUBLESHOOTING FOR THE FOR THE FURTHER ISSUE. HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9846960 ↗
• InjuryFeb 13, 2020Device Alarm System; Excess Flow or Over-Infusion; Mechanical Problem; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem; Device Alarm System; Excess Flow or Over-Infusion; Mechanical Problem; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE CUSTOMER WAS HOSPITALIZED DUE TO SEVERE LOW BLOOD GLUCOSE. IT WAS ALSO REPORTED THAT THE INSULIN PUMP EXPERIENCED SEVERAL MALFUNCTIONS SUCH AS; BATTERY DYING WITHOUT RECEIVING A LOW BATTERY WARING, INSULIN PUMP ADMINISTERING INSULIN WITHOUT PROMPT AND PUMP MAKING LOUD NOISE DURING REWIND. CALLER DID NOT HAVE PERMISSION TO SPEAK ON CUSTOMER¿S BEHALF AND DID NOT WANT CUSTOMER TO SPEAK WITH HELPLINE IN ORDER TO PROVIDE MORE INFORMATION. INSULIN PUMP IS NOT EXPECTED TO RETURN.

  Patient problems: Hypoglycemia

  MAUDE report 9704925 ↗
• MalfunctionFeb 13, 2020Device Difficult to Program or Calibrate; Power Problem; Device Difficult to Program or Calibrate; Power Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP¿S BUTTONS HAD TO BE PRESSED MORE THAN ONCE AND REJECTED A NEW BATTERY. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9703968 ↗
• MalfunctionFeb 7, 2020Mechanical Problem; Mechanical Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER STATED THE DRIVE SUPPORT CAP APPEARS NORMAL. CUSTOMER STATED INSULIN PUMP WAS NOT EXPOSED TO A HIGH MAGNETIC FIELD. CUSTOMER DID NOT REPORT MOTOR POSITION ENCODER ERROR ALARM. CUSTOMER WAS ABLE TO SUCCESSFULLY CLEAR THE ALARM ALSO ABLE TO COMPLETE PUMP REWIND. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9680029 ↗
• MalfunctionJan 30, 2020Premature Discharge of Battery; Power Problem; Premature Discharge of Battery; Power Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP HAD UNEXPECTED RESTART ALARM. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. INSULIN PUMP HAD REJECTED NEW BATTERIES. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9645857 ↗
• MalfunctionJan 10, 2020Device Difficult to Program or Calibrate; Power Problem; Device Difficult to Program or Calibrate; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT BUTTON OF INSULIN PUMP WAS NOT RESPONDING. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER STATED THAT INSULIN PUMP HAD BATTERY OUT LIMIT ALARM. CUSTOMER WAS UNABLE TO CLEAR THE ALARM. CUSTOMER WAS ADVISED TO OBSERVE TIME CLOCK FOR ONE MINUTE TO VERIFY IF TIME ADVANCES AND IT WAS ADVANCES. THE CUSTOMER WAS ADVISED THAT THE INSULIN PUMP NEEDED TO BE REPLACED AND WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND TO REVERT TO THE BACKUP PLAN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9573675 ↗
• MalfunctionDec 20, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP'S DOWN AND UP KEYPAD WAS HARD TO PRESS. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 104 MG/DL. THE CUSTOMER STATED THAT THE TIME ON THE INSULIN PUMP ADVANCED. CUSTOMER WAS ADVISED THAT THE INSULIN PUMP WILL NEED TO BE REPLACED. THE CUSTOMER WAS ADVISED TO DISCONNECT FROM THE INSULIN PUMP AND REVERT TO THE BACKUP PLAN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9502422 ↗
• MalfunctionDec 18, 2019Device Difficult to Program or Calibrate; Obstruction of Flow; Device Difficult to Program or Calibrate; Obstruction of Flow

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD SENSITIVE BUTTONS AND HAD TO BE PRESSED JUST RIGHT BUTTON. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER STATED THAT THEY EXPERIENCED RANDOM AND UNEXPLAINED NO DELIVERY ALERTS. THE CUSTOMER DECLINED THE TROUBLESHOOTING. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9488303 ↗
• MalfunctionDec 18, 2019Device Difficult to Program or Calibrate; Use of Device Problem; Obstruction of Flow; Power Problem; Device Difficult to Program or Calibrate; Use of Device Problem; Obstruction of Flow; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD OCCASIONAL BUTTON ERRORS. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER STATED THAT THE LOSING DATE AND TIME DURING EACH BATTERY CHANGE, HAD TO REPRIME RESERVOIR AFTER EACH BATTERY CHANGE AND RANDOM NO DELIVERY ALERTS. CUSTOMER ALSO STATED THAT THE REJECTED NEW BATTERIES. TROUBLESHOOTING WAS DECLINED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9487316 ↗
• MalfunctionDec 16, 2019Power Problem; Patient Device Interaction Problem; Power Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD FAILED BATTERY TEST ALARM. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER STATED THAT THE CONTACTS WAS NOT MISSING OR DAMAGED AND BATTERY COMPARTMENT WAS DAMAGED AND CORRODED. TROUBLESHOOTING WAS PERFORMED. CUSTOMER WAS ADVISED THAT THE INSULIN PUMP NEEDED TO BE REPLACED AND REVERT TO A BACK-UP PLAN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9471350 ↗
• MalfunctionDec 8, 2019Device Difficult to Program or Calibrate; Obstruction of Flow; Device Difficult to Program or Calibrate; Obstruction of Flow

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP BUTTONS WAS PRESS FIRMLY FOR RESPONSE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER REPORTED THAT THE INSULIN PUMP RECEIVED NO DELIVERY ALARM. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9435212 ↗
• MalfunctionNov 27, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Battery Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Battery Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE BUTTONS OF INSULIN PUMP DID NOT ALWAYS RESPOND AND IT PRESS ONE TO TWO TIMES. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER STATED THAT THERE WAS DIMINISHED BATTERY LIFE AND INSULIN PUMP REWIND SLOWER THAN IT WAS IN THE PAST. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9382154 ↗
• MalfunctionNov 26, 2019Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem

  THE CUSTOMER REPORTED VIA PHONE THAT THE BUTTONS WERE NOT RESPONSIVE. CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF INCIDENT. INSULIN PUMP HAD NO DELIVERY ALARMS. CUSTOMER STATED THAT THE BATTERY SEVERELY DIMINISHED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9375102 ↗
• MalfunctionNov 25, 2019Device Alarm System; Device Difficult to Program or Calibrate; Device Alarm System; Device Difficult to Program or Calibrate

  THE CUSTOMER'S SPOUSE REPORTED VIA PHONE CALL THAT NONE OF THE BUTTONS WERE RESPONDING AND GIVING A HIGH PITCH NOISE. BLOOD GLUCOSE WAS 190 MG/DL. TROUBLESHOOTING WAS PERFORMED AND ACT AND ESC BUTTONS WERE NOT RESPONDING. CUSTOMER ALSO REPORTED THAT TIME WAS ADVANCED. THE CUSTOMER WAS ADVISED THAT THE INSULIN PUMP NEEDED TO BE REPLACED AND WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND TO REVERT TO THE BACKUP PLAN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9373769 ↗
• MalfunctionNov 13, 2019Display or Visual Feedback Problem; Battery Problem; Patient Device Interaction Problem; Display or Visual Feedback Problem; Battery Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP¿S SCREEN WAS SCRATCHED UP AND HARDER TO READ AND GOING THROUGH BATTERIES MORE OFTEN. CUSTOMER'S BLOOD GLUCOSE VALUE WAS UNKNOWN. CUSTOMER DECLINED TO REPORT TO 24 HOURS TECHNICAL SUPPORT DEPARTMENT. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9319350 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P980022. One submission often covers many models, so check the product and lot details in each record.

• Z-1749-2026 · Feb 13, 2026 · Open, Classified
  Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722)
• Z-1750-2026 · Feb 13, 2026 · Open, Classified
  Paradigm REAL-Time Revel Insulin Pump (MMT-523, MMT-723)
• Z-1256-2025 · Jan 31, 2025 · Open, Classified
  Paradigm insulin pump, REF: MMT-522, MMT-523, MMT-551, MMT-722, MMT-723, MMT-751
• Z-1592-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523K
• Z-1588-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-722
• Z-1593-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723K
• Z-1589-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-522K
• Z-1587-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-522
• Z-1591-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523
• Z-1590-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-722K
• Z-1594-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723
• Z-2442-2015 · Jul 22, 2015 · Terminated
  Guardian Real-Time Monitor, Model No. CSS7100. Indicated for continuous or periodic monitoring of glucose levels in the fluid under the skin, in adults (18 years and older) with d
• Z-2179-2014 · Jul 21, 2014 · Terminated
  Medtronic MiniMed Guardian Monitor, Model No. CSS7100, CSS7100K Product Usage: The Medtronic MiniMed model CSS7100 and CSS7100K Guardian REAL-Time monitors are used in combinatio
• Z-2544-2014 · Mar 13, 2014 · Terminated
  Medtronic MiniMed Paradigm Insulin Infusion Pumps, Paradigm models: MMT-511, MMT-512, MMT-712, MMT-712E, MMT-515, MMT-715, MMT-522, MMT-522K, MMT-722, MMT-722K, MMT-523, MMT-523K