PARADIGM® REAL-time MMT-722NAS (UDI 00613994373083)Recalls & reported problems

Summary

The FDA's MAUDE database contains 43 adverse event reports that list this exact device (DI 00613994373083), received between Jul 5, 2017 and May 20, 2020 — classified as 3 deaths, 8 injuries, 32 malfunctions.

The most frequently reported specific device problem is “Failure to Cycle” (9 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 43 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 20, 2020Failure to Cycle; Failure to Cycle

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A COMPROMISED FORCE SENSOR SYSTEM ALARM. THE CUSTOMER STATED THE DEVICE WAS SQUIRTING INSULIN OUT DURING MANUAL PRIME PROCESS. THE DRIVE SUPPORT CAP WAS STICKING OUT. 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 10073505 ↗
• MalfunctionApr 16, 2020Failure to Cycle; Failure to Cycle

  CUSTOMER REPORTED VIA PHONE CALL THE INSULIN PUMP ALARMED COMPROMISED FORCE SENSOR SYSTEM. TROUBLESHOOTING WAS PERFORMED. CUSTOMER BLOOD GLUCOSE READING WAS 105 MG/DL. THE DRIVE SUPPORT CAP WAS PROTRUDED. THE INSULIN PUMP WILL BE RETURNING FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9970003 ↗
• MalfunctionMar 20, 2020Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Power Problem; Patient Device Interaction Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Power Problem; Patient Device Interaction Problem

  IT WAS REPORTED THAT THE CUSTOMER'S WEIGHT HAS BEEN CHANGED TO (B)(6).

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9859079 ↗
• MalfunctionFeb 13, 2020Mechanical Problem; Obstruction of Flow; Mechanical Problem; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER STATED THAT THE INSULIN PUMP HAD NO DELIVERY ALARM. 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 9705000 ↗
• MalfunctionJan 16, 2020Failure of Device to Self-Test; Failure of Device to Self-Test

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY PERFORMED HIGH PRESSURE TEST AND TEST WAS FAILED. THE CUSTOMER¿S BLOOD GLUCOSE WAS 325 MG/DL. CUSTOMER REPORTED THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE. CUSTOMER REPORTED THAT THEY DID NOT ALLEGE INSULIN PUMP WAS UNDER DELIVERING. CUSTOMER WAS NEITHER IN EMERGENCY ROOM, NOR ADMITTED INTO HOSPITAL, NOR WAS EMERGENCY MEDICAL SERVICE DISPATCHED AS A RESULT OF HIGH BLOOD GLUCOSE. CUSTOMER WAS USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE EVENT. CUSTOMER TREATED WITH INSULIN PUMP AND MANUAL INJECTION. CUSTOMER REPORTED THAT THE DRIVE SUPPORT CAP APPEARS NORMAL. CUSTOMER REPORTED THE INSULIN PUMP WAS NOT WORN DURING A MEDICAL PROCEDURE AND TEST AROUND MAGNETIC RESONANCE IMAGING. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING AND DECLINED FOR HIGH BLOOD GLUCOSE. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9594560 ↗
• InjuryJan 15, 2020Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event; Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HYPERGLYCEMIA. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 600 MG/DL, CHANGED INSULIN VIALS THEN CHANGED INSULIN TYPES AND TRIED MANUAL INJECTION AND THIS REDUCED 500 MG/DL AT TIME OF INCIDENT TO 400 MG/DL. CUSTOMER TREATED WITH MANUAL SHOTS. CUSTOMER HAD USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE EVENT. CUSTOMER DOES NOT USE AUTO MODE. CUSTOMER DOES NOT ALLEGE INSULIN PUMP WAS UNDER DELIVERING. CUSTOMER REPORTED THAT THE DRIVE SUPPORT CAP WAS NORMAL. CUSTOMER REPORTED THAT THE INSULIN EXITED AT THE QUICK RELEASE. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9590046 ↗
• DeathDec 26, 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 IN A HOSPITAL EMERGENCY ROOM. THE CUSTOMER WAS HOSPITALIZED ON (B)(6) 2019. THE CAUSE OF DEATH WAS CONGESTIVE HEART FAILURE. THE CALLER STATED THAT THE CUSTOMER HAD BREATHING PROBLEMS AND LUNG CANCER THAT MAY HAVE LED TO THE CUSTOMER'S PASSING. THE CUSTOMER¿S BLOOD GLUCOSE WAS APPROXIMATELY 434 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 WHEN THE CUSTOMER GOT ADMITTED SHORTLY BEFORE PASSING. THE CUSTOMER WAS NOT USING SENSORS. THE CALLER DECLINED TO RETURN THE INSULIN PUMP FOR ANALYSIS.

  Patient problems: Death; Hyperglycemia

  MAUDE report 9518163 ↗
• MalfunctionDec 16, 2019Display or Visual Feedback Problem; Patient Device Interaction Problem; Display or Visual Feedback Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD CRACKED SCREEN AND WAS UNABLE TO READ THE SCREEN. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9472211 ↗
• MalfunctionNov 17, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Patient Device Interaction Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Patient Device Interaction Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP BUTTONS WERE LESS RESPONSIVE, HAD TO PRESS MULTIPLE TIMES. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER STATED INSULIN PUMP HAD CRACKED WHERE RESERVOIR GOES IN FROM TIP TO GLASS ON BOTH SIDES, REWIND TAKES A LITTLE LONGER, RECEIVED UNEXPLAINED NO DELIVERY ALERTS, CHANGES OUT SET COMPLETELY. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9333608 ↗
• MalfunctionNov 11, 2019Mechanical Problem; Power Problem; Patient Device Interaction Problem; Mechanical Problem; Power Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED THAT THE INSULIN PUMP ALARMED MOTOR ERROR, CRACKS, AND PLASTIC PIECE OF RESERVOIR WINDOW COMING OFF. TROUBLESHOOTING WAS NOT PERFORMED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9303505 ↗
• MalfunctionOct 30, 2019Failure to Cycle; Priming Problem; Failure to Cycle; Priming Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN SQUIRTING OUT DURING THE MANUAL PRIME PROCESS. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 194 MG/DL. THE CUSTOMER STATED THAT THE INSULIN PUMP HAD COMPROMISED FORCE SENSOR SYSTEM. CUSTOMER ALSO STATED THAT THEY WAS UNABLE TO EXIT THE PREPARING TO PRIME LOOP. THE CUSTOMER WAS ADVISED THAT THE INSULIN PUMP NEEDED TO BE REPLACED 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 9258482 ↗
• InjuryOct 25, 2019Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event; Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE LEVEL. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 401 MG/DL. CUSTOMER REPORTED THAT THEY RECEIVED NEW BATTERY CAP AND DISPLAY WENT BLANK. CUSTOMER REPORTED THAT THEY WERE ABLE TO CLEAR THE ALARM THAT WAS OCCUR AFTER CHANGING THE BATTERY. CUSTOMER REPORTED THAT THE DISPLAY DID RETURNED. THE INSULIN PUMP WAS ALARMING AT THE TIME OF CALL. THE CUSTOMER WAS ADVISED TO DISCONTINUED THE INSULIN PUMP AND REVERT TO BACKUP PLAN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9239147 ↗
• InjuryOct 25, 2019No Display/Image; No Display/Image

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY HAD HIGH BLOOD GLUCOSE LEVEL. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 401 MG/DL. THE INSULIN PUMP WAS QUIT AFTER PUTTING NEW BATTERY AND HAD BLANK DISPLAY. CUSTOMER WAS NOT CALLING AFTER RECEIVING NEW BATTERY CAP. DISPLAY DID RETURNED. CUSTOMER DID RECEIVED BATTERY OUT LIMIT ALARM AT THE TIME OF CALL. CUSTOMER WAS ABLER TO CLEAR THE ALARM. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9239116 ↗
• MalfunctionSep 18, 2019Failure to Cycle; Detachment of Device or Device Component; Failure to Cycle; Detachment of Device or Device Component

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP ALARMED COMPROMISED FORCE SENSOR SYSTEM. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 140 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER ALSO REPORTED THAT THE INSULIN WAS SQUIRTING DURING MANUAL PRIME PROCESS. THE CUSTOMER STATED THAT THE DRIVE SUPPORT CAP WAS STICKING OUT. 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 9081084 ↗
• MalfunctionAug 14, 2019Failure to Cycle; Priming Problem; Failure to Cycle; Priming Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD A COMPROMISED FORCED SENSOR SYSTEM ERROR. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER ALSO REPORTED THAT THE INSULIN PUMP WAS SQUIRTING OUT INSULIN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8892035 ↗
• MalfunctionAug 13, 2019No Display/Image; Device Difficult to Program or Calibrate; Moisture or Humidity Problem; No Display/Image; Device Difficult to Program or Calibrate; Moisture or Humidity Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD STUCK BUTTON ALERT AND INSULIN PUMP WAS NOT WORKING. CUSTOMER¿S BLOOD GLUCOSE WAS 70 MG/DL. CUSTOMER STATED THAT BUTTONS NOT RESPONDING. CUSTOMER STATED THAT INSULIN PUMP WAS EXPOSURE TO MOISTURE. TROUBLESHOOTING WAS PERFORMED. CUSTOMER WAS ADVISED THAT THE INSULIN PUMP NEEDED TO BE REPLACED AND TO DISCONTINUE USE OF THE INSULIN PUMP 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 8886916 ↗
• MalfunctionJul 11, 2019Device Difficult to Program or Calibrate; Patient Device Interaction Problem; Device Difficult to Program or Calibrate; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP¿S ACT BUTTON WAS NOT RESPONSIVE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER STATED THAT THE INSULIN PUMP WAS NOT HELD TOGETHER BY TAPE AND INSULIN PUMP HAD SCRATCHES ON SCREEN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8779435 ↗
• MalfunctionApr 12, 2019Failure to Cycle; Detachment of Device or Device Component; Failure to Cycle; Detachment of Device or Device Component

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP ALARMED COMPROMISED FORCE SENSOR SYSTEM. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 95 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER ALSO REPORTED THAT THE INSULIN WAS SQUIRTING DURING MANUAL PRIME PROCESS. THE CUSTOMER STATED THAT THE DRIVE SUPPORT CAP WAS STICKING OUT. 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 8507900 ↗
• DeathMar 6, 2019Device Displays Incorrect Message

  IT WAS REPORTED THAT THE CUSTOMER PASSED AWAY IN AN UNKNOWN LOCATION. THE CAUSE OF DEATH WAS UNKNOWN, BUT THERE WAS NO INDICATION THAT A MEDTRONIC PRODUCT CAUSED OR CONTRIBUTED TO THE CUSTOMER'S PASSING. THE NOTIFIER DID NOT STATE WHETHER THE CUSTOMER HAD ANY ILLNESSES THAT MAY HAVE LED TO THE CUSTOMER'S PASSING. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF DEATH. IT IS UNKNOWN IF THE CUSTOMER WAS WEARING THE INSULIN PUMP AT THE TIME OF DEATH. IT IS UNKNOWN IF THE CUSTOMER WAS USING SENSORS. NO FURTHER INFORMATION WAS PROVIDED. THE PUMP WAS RETURNED FOR ANALYSIS. THE PUMP ALARMED MOTOR ERROR ALARM DURING THE BASIC OCCLUSION TEST, AND THE PUMP WAS UNABLE TO PRIME DURING THE PRIME/A33 TEST DUE TO LOOSE/PROTRUDED DRIVE SUPPORT DISK.

  Patient problems: Death

  MAUDE report 7491296 ↗
• MalfunctionFeb 14, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER REPORTED VIA PHONE CALL THAT INSULIN PUMP HAD DRIVE SUPPORT CAP STICKING OUT. 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 8338515 ↗
• MalfunctionDec 7, 2018Patient Device Interaction Problem; Priming Problem; Patient Device Interaction Problem; Priming Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THE INSULIN PUMP INSULIN SQUIRTED OUT IF THE TUBING DURING MANUAL PRIME. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN. THE CUSTOMER INDICATED THE DRIVE SUPPORT CAP WAS NORMAL. THE CUSTOMER 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 8143159 ↗
• MalfunctionDec 5, 2018Device Alarm System; Mechanical Problem; Power Problem; Priming Problem; Device Alarm System; Mechanical Problem; Power Problem; Priming Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD AUDIO VIBRATE ANOMALY AND PRIME ANOMALY. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER STATES INSULIN SQUIRTS DURING PRIME. CUSTOMER ALSO STATES THAT INSULIN PUMP ALSO HAD LOUDER DURING PRIMING AND REWINDING. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8133771 ↗
• MalfunctionNov 15, 2018Failure to Cycle; Failure to Cycle

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP ALARMED COMPROMISED FORCE SENSOR SYSTEM. CUSTOMER'S BLOOD GLUCOSE VALUE WAS 151 MG/DL AT THE TIME OF THE INCIDENT. CUSTOMER STATES THAT THE DRIVE SUPPORT CAP WAS PROTRUDED. THE CUSTOMER WAS ADVISED THE INSULIN PUMP HAS TO BE REPLACED AND REVERT TO BACK-UP PLAN PER HEALTH CARE PROVIDER'S INSTRUCTION. CUSTOMER WILL RETURN THE DEVICE FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8073274 ↗
• MalfunctionOct 10, 2018Unexpected Shutdown; Unexpected Shutdown

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD A PUMP ERROR UNEXPECTED RESTART. A COLD RESET WAS PERFORMED. THE BLOOD GLUCOSE AT THE TIME OF THE INCIDENT WAS 200 MG/DL. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7951041 ↗
• MalfunctionOct 3, 2018Detachment of Device or Device Component; Detachment of Device or Device Component

  CUSTOMER REPORTED VIA PHONE CALL THAT THE DRIVE SUPPORT CAP WAS LOOSE. THE CUSTOMER BLOOD GLUCOSE LEVEL WAS 209 MG/DL AT THE TIME OF INCIDENT. TROUBLESHOOTING WAS PERFORMED. THE PRODUCT WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7929250 ↗

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