Paradigm® REAL-Time Revel™ MMT-723NAP (UDI 00643169077720)Recalls & reported problems

Summary

The FDA's MAUDE database contains 70 adverse event reports that list this exact device (DI 00643169077720), received between Jun 2, 2017 and May 15, 2020 — classified as 2 deaths, 12 injuries, 56 malfunctions.

The most frequently reported specific device problem is “Device Displays Incorrect Message” (17 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 70 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 15, 2020Premature Discharge of Battery; Loss of Data; Premature Discharge of Battery; Loss of Data

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MULTIPLE ERROR ALARM. CUSTOMER DECLINED TROUBLESHOOTING. 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 10060828 ↗
• MalfunctionFeb 28, 2020Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THE INSULIN PUMP HAD BUTTON ERROR WHILE CHANGING RESERVOIR. CUSTOMER REPORTED THAT ALL OF THE BUTTONS WERE NOT RESPONDING. THE TIME ADVANCED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9768246 ↗
• MalfunctionFeb 17, 2020Mechanical Problem; Patient Device Interaction Problem; Mechanical Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM AND CHIPPED NEAR BATTERY COMPARTMENT. 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 9718734 ↗
• MalfunctionDec 19, 2019Failure to Cycle; Detachment of Device or Device Component; Adverse Event Without Identified Device or Use Problem; Failure to Cycle; Detachment of Device or Device Component; Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD DRIVE SUPPORT CAP WAS PROTRUDED AND COMPROMISED FORCE SENSOR SYSTEM ALARM. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 300 MG/DL. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. CUSTOMER REPORTS THEY WERE ABLE TO CLEAR THE ALARM. CUSTOMER ABLE TO COMPLETE REWIND. 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 PER HEALTH CARE PROFESSIONAL INSTRUCTIONS. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9493273 ↗
• MalfunctionNov 25, 2019Mechanical Problem; Obstruction of Flow; Communication or Transmission Problem; Mechanical Problem; Obstruction of Flow; Communication or Transmission Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM DURING BASAL. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 252 MG/DL AT THE TIME OF INCIDENT. CUSTOMER REPORTED THAT THE DRIVE SUPPORT CAP WAS NORMAL. CUSTOMER STATED THAT THE INSULIN PUMP WAS NOT EXPOSED TO HIGH MAGNETIC FIELD. CUSTOMER DID NOT REPORTED MOTOR POSITION ENCODER ERROR ALARM. CUSTOMER STATED THAT THE INSULIN PUMP ALARM HISTORY CONTAINS NEITHER MOTOR POSITION ENCODER ERROR ALARM NOR MORE THAN ONE MOTOR ERROR ALARM WITHIN A 30 DAY PERIOD. CUSTOMER PERFORMED DISPLACEMENT TEST AND IT WAS PASSED. CUSTOMER STATED THAT THE INSULIN PUMP HAD REJECTED NEW BATTERIES, RANDOM UNEXPLAINED NO DELIVERY ALERTS, AND RANDOM INSULIN PUMP FAILURE ALERTS. CUSTOMER STATED THAT THE INSULIN PUMP PASSED MOTOR ERROR TROUBLESHOOTING AND IT WAS WORKING FINE. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9368470 ↗
• MalfunctionOct 16, 2019Detachment of Device or Device Component; No Apparent Adverse Event; Patient Device Interaction Problem; Detachment of Device or Device Component; No Apparent Adverse Event; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT WHEN HE WAS PRIMING THE INSULIN PUMP THE BOTTOM OF THE INSULIN PUMP CAME OFF AND HE CAN NOW SEE THE INSIDE OF THE PUMP. THE BLOOD GLUCOSE WAS 140 MG/DL. THE CUSTOMER REPORTED THAT SEAM SEPARATED. THE DEVICE WILL BE RETURNED FOR THE ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9195470 ↗
• MalfunctionOct 15, 2019Premature Discharge of Battery; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Adverse Event Without Identified Device or Use Problem; Premature Discharge of Battery; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MULTIPLE INSULIN PUMP ISSUES. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN. TROUBLESHOOTING WAS DECLINED FOR INSULIN PUMP ISSUES AND HYPERGLYCEMIA. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9189976 ↗
• MalfunctionOct 4, 2019Failure to Cycle; No Apparent Adverse Event; Failure to Cycle; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP ALARMED COMPROMISED FORCE SENSOR SYSTEM. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER ALSO REPORTED THAT THE INSULIN WAS SQUIRTING. THE CUSTOMER WAS CHANGING RESERVOIR AND LOADING PROCESS WAS NOT WORKING AND MOTOR KEPT ON PUSHING INSULIN. CUSTOMER WAS ABLE TO CLEAR THE ALARM BUT UNABLE TO REWIND THE INSULIN PUMP. THE CUSTOMER WAS ADVISED THAT THE INSULIN PUMP NEEDED TO BE REPLACED AND WAS ADVISED 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 9155342 ↗
• InjurySep 18, 2019Mechanical Problem; Obstruction of Flow; No Apparent Adverse Event; Mechanical Problem; Obstruction of Flow; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 500 MG/DL. THE CUSTOMER DID NOT PROVIDE INFORMATION ABOUT SYMPTOMS AND TREATMENT. THE INSULIN PUMP ALARMED MOTOR ERROR AND INSULIN FLOW BLOCK FOR THE SECOND TIME. CUSTOMER REPORTED THAT THE DRIVE SUPPORT CAP APPEARS NORMAL. CUSTOMER DID NOT REPORT MOTOR POSITION ENCODER ERROR. INSULIN PUMP ALARM HISTORY CONTAINS MORE THAN ONE MOTOR ERROR ALARM WITHIN A 30 DAY PERIOD. THE CUSTOMER WAS TRYING TO CLEAR THE ALARM BUT IT KEEP CAME BACK ON. THE CUSTOMER WAS ADVISED THAT THE PUMP WILL NEED TO BE REPLACED AND WAS ADVISED TO DISCONTINUE USE OF THE PUMP AND REVERT TO A BACK-UP PLAN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9080339 ↗
• MalfunctionSep 11, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Material Integrity Problem; Power Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Material Integrity Problem; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR AND BUTTONS WERE HARDER TO PRESS. THE CUSTOMER'S BLOOD GLUCOSE VALUE WAS UNKNOWN. CUSTOMER STATED INSULIN PUMP0 HAD NO DELIVERY ALERTS, BATTERY CAP WORN AND DIMINISHED BATTERY LIFE. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8991773 ↗
• MalfunctionSep 11, 2019Mechanical Problem; Obstruction of Flow; Mechanical Problem; Obstruction of Flow

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEIR INSULIN PUMP HAD A MOTOR ERROR. THE CUSTOMER¿S BLOOD GLUCOSE WAS 127 MG/DL. CUSTOMER REPORTED THAT THE INSULIN PUMP HAD NO DELIVERY ALARM. CUSTOMER WANTED TO REPLACE THE INSULIN PUMP. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8988817 ↗
• MalfunctionAug 23, 2019Patient Device Interaction Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE LEVEL. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 474 MG/DL. THE CUSTOMER REPORTED THAT THE INSULIN PUMP WAS DAMAGED TO THE BOTTOM. CUSTOMER WAS DECLINED TO TROUBLESHOOT FOR HIGH BLOOD. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 8924973 ↗
• MalfunctionAug 23, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD A MOTOR ERROR ALARM. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER MENTIONED THAT THE DRIVE SUPPORT CAP WAS NORMAL OR SLIGHTLY INDENTED. THE INSULIN PUMP WAS NOT EXPOSED TO HIGH MAGNETIC FIELD. THE CUSTOMER STATED THAT THE ERRORS WOULD OCCUR RANDOMLY. THE CUSTOMER WAS ABLE TO COMPLETE THE INSULIN PUMP REWIND. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND TO REVERT TO THE BACK-UP PLAN. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8924244 ↗
• MalfunctionJul 24, 2019Mechanical Problem; Power Problem; Mechanical Problem; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT INSULIN PUMP HAD MOTOR ERROR AND HAD BUBBLES IN THE LINE AND WAS ABLE TO RESOLVE IT HERSELF AND DID NOT CALL . THE CUSTOMER HAD MORE THAN ONE MOTOR ERROR ALARM WITHIN THE LAST 30 DAYS. THE BLOOD GLUCOSE AT THE TIME OF THE INCIDENT WAS UNKNOWN. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8821313 ↗
• MalfunctionJul 4, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY RECEIVED A BUTTON ERROR. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER STATES THEY WERE NOT ABLE TO CLEAR THE ALARM. THE CUSTOMER REPORTED THAT THE TIME WAS WORKING. THE CUSTOMER WAS ADVISED TO DISCONTINUE THE USE OF INSULIN PUMP AND REVERT TO BACKUP PLAN. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8761758 ↗
• MalfunctionJun 28, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Priming Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Priming Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT HER INSULIN PUMP HAD KEYPAD ANOMALY AND PRIME ANOMALY. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER REPORTED THAT THE BUTTONS WERE HARDER TO PRESS, INSULIN WAS SQUIRTING DURING PRIMING, IT SOUNDED LOUDER WHEN REWINDING, AND SHE HAD RECEIVED NO DELIVERY ALARM TWICE. THE CUSTOMER DECLINED TROUBLESHOOTING. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8743512 ↗
• MalfunctionJun 26, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD A SEVERAL MOTOR ERROR ALARMS. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8733477 ↗
• DeathJun 10, 2019Adverse 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 CAUSE OF DEATH WAS NATURAL CAUSES AS A RESULT OF DIABETES COMPLICATIONS. THE CALLER STATED THAT THE CUSTOMER HAD A NECK SURGERY AND A PROSTHETIC LEG AND NO OTHER ILLNESSES THAT MAY HAVE LED TO THE CUSTOMER'S PASSING. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF DEATH. THE CUSTOMER WAS WEARING THE INSULIN PUMP AT THE TIME OF DEATH. THE CUSTOMER WAS NOT USING SENSORS. THE CALLER DECLINED TO RETURN THE INSULIN PUMP FOR ANALYSIS.

  Patient problems: Death

  MAUDE report 8682169 ↗
• MalfunctionMay 23, 2019Patient Device Interaction Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE BATTERY COMPARTMENT WAS DAMAGED. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF INCIDENT. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8635384 ↗
• MalfunctionApr 25, 2019Mechanical Problem; Battery Problem; Patient Device Interaction Problem; Mechanical Problem; Battery Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MULTIPLE ISSUES. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER STATED THE BUTTONS ON THE INSULIN PUMP WERE GETTING HARD TO USE AND WOULD NOT LET THE CUSTOMER TO ADD WHAT NEEDED INTO THE INSULIN PUMP FOR INSULIN. IT WAS ALSO REPORTED THAT THE BATTERY LIFE WAS NOT LASTING LONG AND HAD TO CHANGE OFTEN. THE CUSTOMER ALSO STATED THAT THE INSULIN PUMP ALSO STOPS REWINDING AND DOES NOT REWIND ALL THE WAY. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8548140 ↗
• MalfunctionMar 29, 2019Mechanical Problem; Battery Problem; Power Problem; Mechanical Problem; Battery Problem; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THE INSULIN PUMP ALARMED MOTOR ERROR. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8463729 ↗
• MalfunctionFeb 28, 2019Device Alarm System; Power Problem; Device Alarm System; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP NO LONGER VIBRATES. THE CUSTOMER ALSO REPORTED THAT THE AUDIO VERY LOW. CUSTOMER REPORTED THAT THE LOW INSULIN INDICATOR DID NOT WORK. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER REPORTED THAT THE DRIVE SUPPORT CAP APPEARS NORMAL. CUSTOMER REPORTED THAT THE BATTERY LIFE DIMINISHING AND ONLY LASTING 6 DAYS. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8376855 ↗
• MalfunctionFeb 22, 2019Date/Time-Related Software Problem; Date/Time-Related Software Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT INSULIN PUMP HAD ERROR OCCURRED TIME AND DATE WAS DIFFERENT. THE BLOOD GLUCOSE AT THE TIME OF THE INCIDENT WAS UNKNOWN. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8360995 ↗
• MalfunctionFeb 5, 2019Device Alarm System; Priming Problem; Device Alarm System; Priming Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD RECEIVED BEEP ANOMALY AS WELL AS INSULIN SQUIRTS OUT. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 250 MG/DL. CUSTOMER ALSO REPORTED THAT THEY DID NOT RECEIVE 2ND SERIES OF BEEPS NOR DID NUMBERS APPEAR ON THE SCREEN. CUSTOMER TROUBLESHOOTING WAS PERFORMED PRIME REWIND. CUSTOMER WAS ADVISED TO THAT THAT THE INSULIN PUMP WILL NEED TO BE REPLACED AND TO REVERT TO BACKUP PLAN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8303758 ↗
• MalfunctionJan 4, 2019Obstruction of Flow; Patient Device Interaction Problem; Obstruction of Flow; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD SCRATCH ON SCREEN AND VIEW WAS HINDERED. THE CUSTOMER'S BLOOD GLUCOSE VALUE WAS UNKNOWN. THE CUSTOMER STATED THAT THE INSULIN PUMP HAD UNEXPLAINED NO DELIVERY ALERTS. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8216247 ↗

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-1593-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723K
• Z-1588-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-722
• 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-1592-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523K
• Z-1589-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-522K
• Z-1594-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723
• Z-1590-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-722K
• 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