Paradigm® REAL-Time Revel™ MMT-723RNAB (UDI 00643169221567)Recalls & reported problems

Summary

The FDA's MAUDE database contains 248 adverse event reports that list this exact device (DI 00643169221567), received between May 24, 2017 and Aug 19, 2020 — classified as 5 deaths, 99 injuries, 144 malfunctions.

The most frequently reported specific device problem is “Device Displays Incorrect Message” (50 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 248 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 19, 2020Mechanical Problem; Mechanical Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR .CUSTOMER WAS ABLE TO CLEAR ALARM AND REWIND. CUSTOMER STATED THAT DRIVE SUPPORT CAP APPEARS NORMAL-SLIGHTLY INDENTED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 10424371 ↗
• InjuryAug 13, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER REPORTED VIA PHONE CALL THAT CUSTOMER WERE EXPERIENCING HIGH BLOOD GLUCOSE. BLOOD GLUCOSE LEVEL AT THE TIME OF THE INCIDENT WAS 400 MG/DL. CUSTOMER STATED DRIVE SUPPORT CAP WAS DAMAGE. CUSTOMER STATED INSULIN PUMP WHOLE BOTTOM CAME OFF. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 10400644 ↗
• MalfunctionJun 25, 2020Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE BUTTON ERROR ALARM. CUSTOMER WAS UNABLE TO CLEAR ALARM. NO HARM A MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10193825 ↗
• MalfunctionJun 24, 2020Display or Visual Feedback Problem; Display or Visual Feedback Problem

  CUSTOMER REPORTED VIA PHONE CALL PARTIAL DISPLAY ON THE INSULIN PUMP. TROUBLESHOOTING WAS PERFORMED. CUSTOMER ADVISED THEY WERE UNABLE TO SEE THEIR DISPLAY SCREEN. 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 10188147 ↗
• MalfunctionJun 15, 2020Display or Visual Feedback Problem; Device Difficult to Program or Calibrate; Moisture or Humidity Problem; Display or Visual Feedback Problem; Device Difficult to Program or Calibrate; Moisture or Humidity Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP HAD BUTTON ERROR ALARM AND BUTTONS WERE NOT RESPONDING. CUSTOMER REPORTED THAT INSULIN PUMP WAS EXPOSED TO MOISTURE AND BLACK SOLID CIRCLE WAS FOUND IN INSULIN PUMP. 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 10151900 ↗
• MalfunctionMay 29, 2020Premature Discharge of Battery; Device Difficult to Program or Calibrate; Premature Discharge of Battery; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD UNEXPECTED RESTART AND A COLD RESET WAS PERFORMED. CUSTOMER REPORTED THAT THEY WERE NOT ABLE TO CLEAR THE ALARM. ALSO THE ESCAPE BUTTON WAS NOT RESPONDING. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10100571 ↗
• MalfunctionMar 3, 2020Display or Visual Feedback Problem; Device Difficult to Program or Calibrate; Battery Problem; Display or Visual Feedback Problem; Device Difficult to Program or Calibrate; Battery Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP ACT BUTTON WAS UNRESPONSIVE. CUSTOMER STATED SCREEN STARTING TO FADE AND VERY HARD TO READ FULL DISPLAY. CUSTOMER STATED INSULIN PUMP BATTERY LIFE DIMINISHED. 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 9778987 ↗
• MalfunctionFeb 12, 2020Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Power Problem; Insufficient Device Problem Information; Patient Device Interaction Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Power Problem; Insufficient Device Problem Information; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP BUTTONS HARDER TO PUSH AND RANDOM ERROR MESSAGES. THE CUSTOMER STATED THAT THE INSULIN PUMP HAD SCRATCHES ON SCREEN WHICH WAS HARDER TO READ AND LOUDER REWIND. CUSTOMER STATED INSULIN PUMP REJECT NEW BATTERIES AND UNEXPLAINED NO DELIVERY ALERTS. 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 9698774 ↗
• MalfunctionFeb 6, 2020Power Problem; Power Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD OFF NO POWER ALARM. CUSTOMER STATED THEY DID NOT RECEIVED LOW BATTERY ALERT PRIOR TO REPLACE BATTERY ALARM. CUSTOMER STATED THIS WAS NOT THE SECOND OCCURRENCE OF OFF NO POWER WITHOUT A LOW BATTERY WARNING. 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 9675537 ↗
• MalfunctionDec 27, 2019Mechanical Problem; Environmental Compatibility Problem; Mechanical Problem; Environmental Compatibility Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 143 MG/DL. THE CUSTOMER STATED THAT HER INSULIN PUMP HAS STOPPED WORKING AND SAYS MOTOR ERROR ON THE SCREEN. THE TROUBLESHOOTING WAS PERFORMED FOR THE MOTOR ERROR ALARM. CUSTOMER REPORTED THAT THE DRIVE SUPPORT CAP WAS APPEARED NORMAL. CUSTOMER WAS ABLE TO SUCCESSFULLY CLEAR THE ALARM. CUSTOMER WAS UNABLE TO COMPLETE INSULIN PUMP REWIND. THE CUSTOMER STATED THAT THE INSULIN PUMP HAS BEEN EXPOSED TO HIGH MAGNETIC FIELD. THE CUSTOMER WAS ADVISED THAT THE INSULIN PUMP WILL NEED TO BE REPLACED. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND REFER TO BACK UP PLAN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9522568 ↗
• MalfunctionDec 18, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD KEYPAD ISSUES. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 129 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER WAS REPORTED THAT WHEN THEY TRIED TO PUSH THE BUTTONS NOTHING HAPPENED. CUSTOMER WAS CHANGED THE BATTERY STILL INSULIN PUMP WAS FREEZE. THE CUSTOMER WAS ADVISED TO REPLACE AND 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: No Consequences Or Impact To Patient

  MAUDE report 9487475 ↗
• InjuryDec 12, 2019Excess Flow or Over-Infusion; No Apparent Adverse Event; Excess Flow or Over-Infusion; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE CUSTOMER EXPERIENCED HYPERGLYCEMIA AND WAS HOSPITALIZED THREE TIMES DUE TO OVER AND UNDER DOSES. THE CUSTOMER HIGH BLOOD GLUCOSE LEVEL WAS IN RANGE 55 MG/DL TO 300 MG/DL. CUSTOMER HAS BEEN EXPERIENCING LOW BLOOD GLUCOSE FOR ABOUT 2 MONTHS. CUSTOMER HAS BEEN USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE EVENT. CUSTOMER STATED THE DRIVE SUPPORT CAP APPEARED NORMAL. CUSTOMER DOES ALLEGED INSULIN PUMP WAS OVER DELIVERING. CUSTOMER TREATED FOR USING LIBRE CONTINUOUS GLUCOSE MONITORING. THE INSULIN PUMP, RESERVOIR AND INFUSION SET WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia; Hypoglycemia

  MAUDE report 9456272 ↗
• MalfunctionNov 16, 2019Device Difficult to Program or Calibrate; Patient Device Interaction Problem; Device Difficult to Program or Calibrate; Patient Device Interaction Problem

  THE CUSTOMER'S EDUCATOR REPORTED VIA PHONE CALL THAT THEIR INSULIN PUMP HAD CRACK NEAR ACT BUTTON AND AIR BUBBLES IN THE RESERVOIR. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER STATED THAT CRACK ON CASE AND ACT WONT ENGAGE AT ALL AND SHE CANNOT BOLUS AT ALL AND BIG AIR BUBBLE IN RESERVOIR. CUSTOMER WAS DECLINED TROUBLESHOOTING FOR AIR BUBBLE. 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 AND RESERVOIR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9332617 ↗
• MalfunctionNov 11, 2019Display or Visual Feedback Problem; Device Difficult to Program or Calibrate; Display or Visual Feedback Problem; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD PARTIAL DISPLAY AND BUTTONS WERE HARD TO PRESS. THE CUSTOMER'S BLOOD GLUCOSE VALUE WAS UNKNOWN. CUSTOMER STATED THAT THE DISPLAY RETURNED TO NORMAL. CUSTOMER WAS ASSISTED TO PERFORM SELF TEST. CUSTOMER DECLINED TO FURTHER TROUBLESHOOTING. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9307829 ↗
• MalfunctionOct 26, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE THAT INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER¿S BLOOD GLUCOSE WAS 137 MG/DL AT THE TIME OF INCIDENT. DRIVE SUPPORT CAP WAS NORMAL. INSULIN PUMP HAS NOT BEEN EXPOSED TO HIGH MAGNETIC FIELD. CUSTOMER WAS ABLE TO SUCCESSFULLY CLEAR THE ALARM. CUSTOMER WAS UNABLE TO COMPLETE PUMP 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. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9243216 ↗
• MalfunctionOct 9, 2019Power Problem; Priming Problem; Power Problem; Priming Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY WERE NOT ABLE TO REWIND THE INSULIN PUMP. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF INCIDENT. CUSTOMER STATED THAT THE INSULIN PUMP WAS DIED AND RESERVOIR WAS EMPTY AND BATTERY WAS DEAD. CUSTOMER STATED THAT THE INSULIN WAS SQUIRTING OUT DURING THE MANUAL PRIME PROCESS. CUSTOMER WAS NOT ABLE TO ESCAPE TO THE STATUS SCREEN. CUSTOMER STATED THAT THE INSULIN PUMP HAD BATTERY OUT LIMIT AND INSULIN PUMP WAS STUCK IN REWIND LOOP. CUSTOMER WAS ABLE TO CLEAR THE ALARM. THE CUSTOMER WAS ADVISED THAT THE INSULIN PUMP NEEDED TO BE REPLACED AND REVERT TO THE BACKUP PLAN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9170385 ↗
• InjuryOct 5, 2019Obstruction of Flow; Obstruction of Flow

  THE CUSTOMER REPORTED VIA PHONE CALL THAT CUSTOMER EXPERIENCED HYPERGLYCEMIA. THE CUSTOMER BLOOD GLUCOSE LEVEL WAS 465 MG/DL AND AROUND 400 MG/DL. CUSTOMER DECLINED TROUBLESHOOTING. CUSTOMER STATED INSULIN PUMP HAD NO DELIVERY ALERTS. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia; Pain

  MAUDE report 9159847 ↗
• MalfunctionSep 12, 2019Display or Visual Feedback Problem; Obstruction of Flow; Battery Problem; Power Problem; Patient Device Interaction Problem; Display or Visual Feedback Problem; Obstruction of Flow; Battery Problem; Power Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE THAT THE INSULIN PUMP SCREEN WAS DARK AND HARD TO READ. CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF INCIDENT. CUSTOMER STATED THAT THE INSULIN PUMP HAD NO DELIVERY ALARM. CUSTOMER STATED THAT THE INSULIN PUMP REJECTED NEW BATTERIES. CUSTOMER STATED THAT THERE WAS CHIPPING IN THE CASE OF INSULIN PUMP. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9001069 ↗
• MalfunctionSep 10, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Material Integrity Problem; Patient Device Interaction Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Material Integrity Problem; Patient Device Interaction Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP'S BUTTONS WERE NOT WORKING UNLESS PRESSED MULTIPLE TIMES. CUSTOMER'S BLOOD GLUCOSE VALUE WAS UNKNOWN. THE INSULIN PUMP WAS LOUDER TO REWIND AND HAD UNEXPLAINED RANDOM NO DELIVERY ALARMS. CUSTOMER DECLINED TO TROUBLESHOOTING. INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8980898 ↗
• MalfunctionAug 28, 2019Mechanical Problem; Patient Device Interaction Problem; Mechanical Problem; 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 AT THE TIME OF THE INCIDENT. CUSTOMER STATED THAT RESERVOIR AREA WAS BROKEN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8938824 ↗
• MalfunctionAug 23, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP ALARMED BUTTON ERROR. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS NOT REPORTED. CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE DEVICE AND REVERT TO A BACKUP PLAN. THE CUSTOMER WAS ADVISED THAT THE DEVICE WOULD BE REPLACED AND AGREED TO RETURN THE PRODUCT FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8924816 ↗
• MalfunctionAug 22, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP¿S BUTTON HAD HARD TO PRESS. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 175 MG/DL. CUSTOMER REPORTED THAT ACT BUTTON DID NOT WORK. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8919777 ↗
• MalfunctionAug 22, 2019Device Alarm System; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Power Problem; Insufficient Device Problem Information; Patient Device Interaction Problem; Device Alarm System; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Power Problem; Insufficient Device Problem Information; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE BUTTONS OF INSULIN PUMP WAS STICKY AND NON RESPONSIVE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER STATED THAT THE INSULIN PUMP HAD UNEXPLAINED NO DELIVERY ALARM AND BUTTON ERROR. THE CUSTOMER STATED THAT THE INSULIN PUMP HAD UNSPECIFIED PUMP ERROR AND SUDDEN POWER DOWN WITHOUT LOW BATTERY WARNING. CUSTOMER STATED THAT SCREEN OF INSULIN PUMP HAD CRACK AND IT HARD TO SEE SCREEN. CUSTOMER ALSO STATED THAT GRINDING DURING REWIND PROCESS. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8919323 ↗
• MalfunctionAug 21, 2019Mechanical Problem; Priming Problem; Mechanical Problem; Priming Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY ARE UNABLE TO EXIT THE PREPARING TO PRIME LOOP. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. 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 DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8914797 ↗
• MalfunctionAug 20, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT ACT BUTTON ON THE INSULIN PUMP WAS NOT RESPONDING. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 175 MG/DL. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8909255 ↗

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-1750-2026 · Feb 13, 2026 · Open, Classified
  Paradigm REAL-Time Revel Insulin Pump (MMT-523, MMT-723)
• Z-1749-2026 · Feb 13, 2026 · Open, Classified
  Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722)
• 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-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-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-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-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