Paradigm® REAL-Time Revel™ MMT-723RNAB (UDI 00613994904423)Recalls & reported problems

Summary

The FDA's MAUDE database contains 28 adverse event reports that list this exact device (DI 00613994904423), received between Jul 10, 2017 and Mar 31, 2020 — classified as 1 death, 11 injuries, 16 malfunctions.

The most frequently reported specific device problem is “Device Displays Incorrect Message” (7 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 28 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 31, 2020No Display/Image; Obstruction of Flow; Patient Device Interaction Problem; No Display/Image; Obstruction of Flow; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE SCREEN WAS SCRATCHED AND HARD TO READ AT TIMES. CUSTOMER ALSO STATED THAT THE INSULIN PUMP HAD AN UNEXPLAINED NO DELIVERY ALARMS. 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 9902370 ↗
• MalfunctionFeb 12, 2020Obstruction of Flow; Date/Time-Related Software Problem; Patient Device Interaction Problem; Obstruction of Flow; Date/Time-Related Software Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE SCREEN OF INSULIN PUMP HAD SCRATCHES AND THEY WERE UNABLE TO READ. CUSTOMER ALSO REPORTED THAT INSULIN PUMP HAD TIME CLOCK ANOMALY AND NO DELIVERY ALARM. SELF TEST WAS PERFORMED AND IT WAS PASSED. 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 9703832 ↗
• MalfunctionSep 2, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  CUSTOMER REPORTED VIA PHONE CALL THAT CUSTOMER WAS UNABLE TO CLEAR ACTIVE ALARM. CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN. CUSTOMER STATED THAT INSULIN PUMP HAD LOW RESERVOIR MESSAGE AND SHE PRESS ESC AND THEN ACT BUTTON BUT IT DID NOT CLEAR THE ALARM. CUSTOMER STATED TIME ADVANCES AFTER WAITING FOR ONE MINUTE. CUSTOMER WAS ADVISED DISCONTINUE USE OF THE PUMP. RECOMMENDED CUSTOMER REFER TO BACK UP PLAN. INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8954202 ↗
• MalfunctionAug 21, 2019Device Alarm System; Device Difficult to Program or Calibrate; Battery Problem; Device Alarm System; Device Difficult to Program or Calibrate; Battery Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP ALARM HAD LOST SOME OF IT WAS LOUDNESS, UP AND DOWN BUTTONS HAD TO PRESS MULTIPLE TIMES AND BATTERIES ONLY LASTING TWO TO THREE. CUSTOMER'S BLOOD GLUCOSE VALUE WAS UNKNOWN. CUSTOMER DECLINED TO REPORT HELPLINE PORTAL. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8914038 ↗
• InjuryApr 30, 2019Obstruction of Flow; Power Problem; No Apparent Adverse Event; Obstruction of Flow; Power Problem; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY HAD A HIGH BLOOD GLUCOSE AND INSULIN PUMP HAD NO DELIVERY ALARM. THE CUSTOMER BLOOD GLUCOSE VALUE WAS 459 MG/DL. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING STEPS. THE CUSTOMER STATED THAT INSULIN EXITS WITH THE MANUAL PRIME. THE CUSTOMER STATES THAT THEY WERE ABLE TO ASSEMBLE A NEW INFUSION SET AND RESERVOIR. THE CUSTOMER STATES THEY DID NOT RECEIVE FAILED BATT TEST AND CUSTOMER STATES THE PUMP ALARMED AFTER BATTERY CHANGE. THE CUSTOMER ABLE TO CLEAR THE ALARM AND THEY DID NOT RECEIVE A REQUEST TO REWIND PUMP. THE CUSTOMER STATED THAT BATTERIES WERE OUT OF PUMP GREATER THAN DURATION ALLOWED BY THE PUMP. THE CUSTOMER WAS DECLINED TROUBLESHOOTING FOR HIGH BLOOD GLUCOSE. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 8563530 ↗
• MalfunctionMar 11, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER REPORTS THEY WERE ABLE TO CLEAR THE ALARM. CUSTOMER STATES THEY ARE NOT ABLE TO REWIND THE INSULIN PUMP. CUSTOMER STATES DRIVE SUPPORT CAP APPEARS TO BE NORMAL. CUSTOMER ADVISED THE PUMP WILL NEED TO BE REPLACED. ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8407122 ↗
• MalfunctionFeb 11, 2019Excess Flow or Over-Infusion; Excess Flow or Over-Infusion

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

  Patient problems: Hypoglycemia

  MAUDE report 8328180 ↗
• InjuryDec 14, 2018Mechanical Problem; Mechanical Problem

  THE CUSTOMER'S SON WAS REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR. THE CUSTOMER¿S CURRENT BLOOD GLUCOSE LEVEL WAS 333 MG/DL. THE DRIVE SUPPORT CAP WAS NORMAL. CUSTOMER WAS ABLE TO COMPLETE INSULIN PUMP REWIND. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND TO REVERT TO THE BACK-UP PLAN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 8163641 ↗
• MalfunctionNov 5, 2018Mechanical Problem; Obstruction of Flow; Patient Device Interaction Problem; Mechanical Problem; Obstruction of Flow; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER REPORTED THAT THE SCRATCH ON THE SCREEN THAT INTERFERES WITH NUMBERS ON THE SCREEN, MULTIPLE RANDOM NO DELIVERY ALARMS, AND ALSO HAD MOTOR ERROR. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8037152 ↗
• InjuryNov 1, 2018No Apparent Adverse Event; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY WERE HOSPITALIZED DUE TO HIGH BLOOD GLUCOSE ON (B)(6) "2012" WITH BLOOD GLUCOSE OF 1450 MG/DL. THE CUSTOMER DID NOT EXPERIENCE ANY SYMPTOMS SUCH AS A RESULT OF HIGH BLOOD GLUCOSE. THE CUSTOMER STATED THAT INSULIN PUMP WAS NOT DELIVERING THE INSULIN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 8030158 ↗
• DeathOct 29, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE CUSTOMER PASSED AWAY IN AN UNKNOWN LOCATION. THE CAUSE OF DEATH WAS UNKNOWN). THE CALLER STATED THAT THEY DID NOT KNOW IF THE CUSTOMER HAD ANY 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 NOT WEARING THE INSULIN PUMP AT THE TIME OF DEATH. THE INSULIN PUMP HAD BEEN DISCONNECTED OVER 2 YEARS PRIOR TO PASSING. THE CUSTOMER'S HEALTH CARE PROFESSIONAL TOLD THE CUSTOMER TO STOP USING THE PUMP AS THEY WERE HAVING LOW BLOOD GLUCOSE LEVELS. THE CALLER WAS UNSURE IF THE CUSTOMER WAS USING SENSORS. THE CALLER DECLINED TO RETURN THE INSULIN PUMP FOR ANALYSIS.

  Patient problems: Death; Hypoglycemia

  MAUDE report 8017689 ↗
• MalfunctionOct 22, 2018Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD REWINDING TOOK LONGER AND REWINDING SOUND LOUDER. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER RECEIVED MOTOR ERROR ALARM. TROUBLESHOOT WAS NOT PERFORMED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7989042 ↗
• MalfunctionJul 18, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP REJECT NEW BATTERIES, SQUIRTING INSULIN ON PRIMING AND RESERVOIR OCCASIONALLY LOOSE WHEN HE GOES TO CHANGE IT. 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 7701045 ↗
• MalfunctionJul 16, 2018Obstruction of Flow; Obstruction of Flow

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD AN UNEXPECTED NO DELIVERY ALARM. THE CUSTOMER STATED WHEN SHE DID A REGULAR SET CHANGE IT GAVE HER A NO DELIVERY MULTIPLE TIMES WHICH LED HER TO CHANGE QUICK SET AGAIN AND RECEIVED ANOTHER NO DELIVERY ALARM. BLOOD GLUCOSE VALUE WAS UNKNOWN AT THE TIME OF THE INCIDENT. TROUBLESHOOTING WAS NOT PERFORMED BECAUSE THE CUSTOMER DECLINED. THE DEVICE WILL BE REPLACED AND RETURNED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7688911 ↗
• MalfunctionJun 29, 2018Failure to Prime

  CUSTOMER REPORTED VIA PHONE CALL THAT INSULIN PUMP HAD PRIME REWIND. 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 7650976 ↗
• MalfunctionJun 5, 2018Device Displays Incorrect Message

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP COMPRISED FORCE SENSOR SYSTEM ERROR ALARM. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 301 MG/DL AT THE TIME OF THE INCIDENT. ALARM OCCURRED DURING THE REWIND. THE PRODUCT WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 7568799 ↗
• InjuryFeb 27, 2018Device Displays Incorrect Message

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY HAD HIGH BLOOD GLUCOSE. THE CUSTOMER'S BLOOD GLUCOSE WAS 300 MG/DL AND CURRENT IS 488 MG/DL AND GONE UP TO 596 MG/DL. THE CUSTOMER DECLINED TROUBLESHOOTING ON INSULIN PUMP. THE CUSTOMER REPORTED THAT THEY RECEIVED NO DELIVERY ALARM AND INSULIN WAS EXITED DURING PRIME. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 7301484 ↗
• InjuryFeb 16, 2018Failure to Deliver

  THE CUSTOMER¿S WIFE REPORTED VIA PHONE CALL THAT HER HUSBAND HAD AND THE PUMP HAD EXPERIENCED HIGH BLOOD GLUCOSE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 423 MG/DL 382 MG/DL AND 261 MG/DL. IT WAS REPORTED THAT THEY HAD NO DELIVERY AND PERFORMED PRIME A 5 UNITS FIXED PRIME/FILL CANNULA AND THE INSULIN EXITED. THE CUSTOMER WAS ADVISED THAT THE SITE MAY HAVE BEEN OCCLUDED AND TO CHANGE THE ENTIRE INFUSION SET SYSTEM. THE CUSTOMER WAS ADVISED TO RESET FIXED PRIME TO THE APPROPRIATE CANNULA PRIME FOR THEIR INFUSION. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 7279016 ↗
• InjuryDec 11, 2017Loss of Power; Device Displays Incorrect Message

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP KEPT SHUTTING OFF. THE DEVICE STARTED BEEPING AND THE DEVICE WOULD SHUT OFF. THE CUSTOMER¿S BLOOD GLUCOSE DURING THE INCIDENT WAS 136 MG/DL. TROUBLESHOOTING WAS NOT PERFORMED. ADDITIONALLY, THE CUSTOMER STATED THEY WOKE UP WITH A HIGH BLOOD GLUCOSE. THE CUSTOMER ALSO REPORTED THAT THEY WOULD USUALLY WAKE UP WITH A LOW BLOOD GLUCOSE BETWEEN 30 MG/DL AND 50 MG/DL. THE CUSTOMER STATED THEIR HIGH AND LOW BLOOD GLUCOSE WAS DUE TO DEVICE SETTING ADJUSTMENTS. THE ALARM HISTORY CONTAINED TWO NO DELIVERY ALARMS AND ONE MOTOR ERROR ALARM. THE INSULIN PUMP IS NOT EXPECTED TO RETURN FOR ANALYSIS.

  Patient problems: Hyperglycemia; Hypoglycemia

  MAUDE report 7107058 ↗
• InjurySep 21, 2017Leak/Splash

  CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE LEVEL OF 500 MG/DL. CUSTOMER DECLINED TO TROUBLESHOOT FOR HIGH READINGS. THE CUSTOMER STATED THAT THERE WAS LEAK AT THE QUICK RELEASE OF THE INFUSION SET. THE PRODUCT WAS NOT RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 6882702 ↗
• InjurySep 11, 2017Failure to Power Up; Device Displays Incorrect Message

  THE CUSTOMER REPORTED VIA PHONE CALL ON THAT THE INSULIN PUMP ALARMED OFF NO POWER. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 426 MG/DL AT THE TIME OF THE INCIDENT. NO SYMPTOMS NOTED FOR THE HYPERGLYCEMIA, BUT THE CUSTOMER TREAT IT WITH THE INSULIN PUMP. THE CUSTOMER NOTED THAT WHILE HE WAS SELF-DELIVERING A BOLUS, THE DEVICE KEPT TELLING HIM TO CHANGE THE BATTERY. CUSTOMER DID RECEIVE A LOW BATTERY ALARM, AND WAS ABLE TO FIX IT WITH A NEW BATTERY. THE CUSTOMER REPORTED THAT THE INSULIN PUMP WOULD NOT TURN ON. THE CUSTOMER WAS ADVISED TO MONITOR THE DEVICE, AND THAT A REPLACEMENT BATTERY CAP WILL BE SENT OUT AS A PRECAUTION. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 6856647 ↗
• MalfunctionAug 4, 2017Device Displays Incorrect Message

  THE CUSTOMER REPORTED VIA PHONE CALL THE INSULIN PUMP ALARMED LOW BATTERY. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 346 MG/DL AT THE TIME OF THE INCIDENT. THE ALARM WAS NOT RESOLVED DURING TROUBLESHOOTING. THE ALARM OCCURRED AFTER INSERTING A NEW BATTERY. ADVISED TO DISCONTINUE USE OF THE PUMP AND REVERT TO A BACK-UP PLAN PER HCP'S INSTRUCTION. ADVISED THE PUMP WILL NEED TO BE REPLACED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 6767552 ↗
• MalfunctionJul 26, 2017No Display/Image

  CUSTOMER CALLED TO REPORT THAT THE INSULIN PUMP HAS A BLANK DISPLAY. CUSTOMER'S BLOOD GLUCOSE READING AT THE TIME OF THE INCIDENT WAS NOT INCLUDED IN THE REPORT. CUSTOMER REPORTED THAT THE ISSUE REMAINED UNRESOLVED AFTER THE BATTERY WAS CHANGED. PRODUCT IS NOT EXPECTED TO RETURN.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 6745620 ↗
• MalfunctionJul 14, 2017No Display/Image; Moisture Damage

  IT WAS REPORTED VIA PHONE CALL THAT THEIR INSULIN PUMP WAS EXPOSED TO MOISTURE; THE CUSTOMER JUMPED INTO THE POOL WHILE WEARING THE DEVICE. THE PATIENT'S BLOOD GLUCOSE AT THE TIME OF INCIDENT IS UNKNOWN. TROUBLESHOOTING WAS INITIATED FOR THE EXPOSURE TO MOISTURE AND THE CALLER CONFIRMED THAT THE INSULIN PUMP WENT BLANK. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND REVERT TO A BACK-UP PLAN PER HEALTH CARE PROFESSIONAL'S INSTRUCTION. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6715526 ↗
• InjuryJul 12, 2017Bent

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY WERE HOSPITALIZED DUE TO A HIGH BLOOD GLUCOSE ON (B)(6) 2017. THE CUSTOMER'S SON REPORTED HIGH BLOOD GLUCOSE LEVELS THAT WERE NOT COMING DOWN AND THE CUSTOMER ENDED UP IN THE HOSPITAL FOR A COUPLE OF DAYS. THE BLOOD GLUCOSE VALUE AT THE TIME OF ADMISSION 600+ MG/DL. THE CUSTOMER HAD SYMPTOMS OF NAUSEA, VOMITING AND CHEST PAINS. THE CUSTOMER TREATED FOR THE HIGH BLOOD GLUCOSE LEVEL WITH THE INSULIN PUMP THROUGHOUT THE NIGHT AND IN THE MORNING STARTED WITH MANUAL INJECTIONS. THE CUSTOMER WAS WEARING THE PUMP AT THE TIME OF THE HOSPITALIZATION. THE CUSTOMERS CURRENT BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE TECHNICIAN PERFORMED TROUBLESHOOTING AND CONFIRMED THE INSULIN PUMP IS WORKING AS DESIGNED. THE INFUSION SETS WHERE CHANGED 2 TIMES AND FOUND ONE OF THE CANNULAS BENT. THE CUSTOMER WAS ADVISED TO CHANGE THE ENTIRE SET, RESERVOIR AND INSULIN AND TREAT PER THE HEALTHCARE PROVIDER'S INSTRUCTIONS. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Chest Pain; Hyperglycemia; Nausea; Vomiting

  MAUDE report 6708608 ↗

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-1594-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723
• Z-1593-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723K
• Z-1591-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523
• Z-1588-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-722
• Z-1590-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-722K
• 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-1592-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523K
• 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