Paradigm® REAL-Time Revel™ MMT-723NAB (UDI 00613994904317)Recalls & reported problems

Summary

The FDA's MAUDE database contains 48 adverse event reports that list this exact device (DI 00613994904317), received between Jun 9, 2017 and Jul 25, 2023 — classified as 10 injuries, 38 malfunctions.

The most frequently reported specific device problem is “Device Displays Incorrect Message” (16 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 48 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 25, 2023Break; Obstruction of Flow; Break; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE CUSTOMER REPORTED CRACK IN PUMP CASING AT BATTERY CAP AREA AND SCREEN WAS CRACKED AND THE PATIENT WAS UNABLE TO SEE THE FULL SCREEN. CUSTOMER ALSO REPORTED RANDOM NO DELIVERY ALARMS. TROUBLESHOOTING WAS NOT PERFORMED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WILL DISCONTINUE USING THE INSULIN PUMP AND THE PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17386624 ↗
• MalfunctionJul 15, 2020Mechanical Problem; Material Integrity Problem; Mechanical Problem; Material Integrity Problem

  INFORMATION RECEIVED BY MEDTRONIC A THAT THE INSULIN PUMP HAD MOTOR ERROR. 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 10275981 ↗
• InjuryJun 30, 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 HIGH BLOOD GLUCOSE. BLOOD GLUCOSE READING WENT UP TO 529 MG/DL. CUSTOMER WAS TREATED FOR THEIR HIGH BLOOD GLUCOSE WITH SYRINGE. CUSTOMER STATED THAT THEY PERFORMED SELF TEST AND DISPLACEMENT TEST AND BOTH WERE PASSED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 10211611 ↗
• MalfunctionFeb 27, 2020Application Program Version or Upgrade Problem; Loss of Data; Application Program Version or Upgrade Problem; Loss of Data

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD NEW SOFTWARE RELEASE DETECTED ERROR ALARM. THE CUSTOMER STATED INSULIN PUMP DID NOT RECEIVED A SECOND ALARM AFTER CLEARING THE INITIAL ALARM. CUSTOMER REPORTED INSULIN PUMP RESTARTED AND GOT ERROR FAILURE OF FLASH MEMORY ERROR ALARM. CUSTOMER REPORTED THEY WERE UNABLE TO CLEAR THE ALARM. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9762341 ↗
• MalfunctionJan 29, 2020Failure 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

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A COMPROMISED FORCE SENSOR SYSTEM ALARM. THE INSULIN PUMP WAS NOT BUMPED OR DROPPED PRIOR TO THE ALARM AND 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 9641047 ↗
• MalfunctionJan 10, 2020Failure 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 UNKNOWN. CUSTOMER STATED THAT THE DRIVE SUPPORT CAP WAS STICKING OUT. THE CUSTOMER WAS ADVISED THAT THE INSULIN PUMP NEEDED TO BE REPLACED. DEVICE WILL BE RETURNED FOR THE ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9573953 ↗
• MalfunctionJan 3, 2020Failure 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 HAD COMPROMISED FORCE SENSOR SYSTEM ALARM. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 248 MG/DL. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. CUSTOMER STATED THAT DRIVE SUPPORT CAP WAS STICKING OUT. 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 9545077 ↗
• MalfunctionDec 23, 2019Material Integrity Problem; Patient Device Interaction Problem; Material Integrity Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE RING WAS DAMAGED AT RESERVOIR COMPARTMENT. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER ALSO STATED THAT THE BATTERY CAP WAS CHIPPED OFF, BATTERY CAP WAS HARD TO SCREW ON, PIECE WAS MISSING AT BATTERY CASING. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9514328 ↗
• MalfunctionNov 20, 2019No Display/Image; Patient Device Interaction Problem; No Display/Image; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP WAS NOT TURNING ON WITH SEVERAL FRESH BATTERY CHANGES. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER REPORTED THAT INSULIN PUMP HAD CRACK ON DISPLAY SCREEN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9346832 ↗
• MalfunctionSep 17, 2019Mechanical Problem; Unexpected Therapeutic Results; Mechanical Problem; Unexpected Therapeutic Results

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERRORS. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN. CUSTOMER STATED THAT THE ABLE TO DELIVER FOUR UNITS PER BOLUS AND TO ENTER MULTIPLE BOLUSES AT ONE TIME. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9076261 ↗
• MalfunctionAug 23, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD BUTTON ERROR ALARM. THE CUSTOMER¿S BLOOD GLUCOSE WAS 220 MG/DL AT THE TIME OF INCIDENT. THE CUSTOMER ALSO STATED THAT BUTTONS WERE NOT RESPONDING. THE CUSTOMER WAS ADVICE THE INSULIN PUMP WILL NEED TO BE REPLACED. ADVICE TO DISCONTINUE USE OF THE INSULIN PUMP AND REVERT TO BACKUP PLAN PER HEALTH CARE PROFESSIONAL INSTRUCTIONS. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8924382 ↗
• MalfunctionJul 16, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE DRIVE SUPPORT CAP OF INSULIN PUMP WAS LOOSE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER STATED THAT THE INSULIN PUMP WAS DROPPED. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND WAS ADVISED THAT THE INSULIN PUMP NEEDED TO BE REPLACED AND FOLLOW THE BACKUP PLAN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8792231 ↗
• MalfunctionJul 12, 2019Premature Discharge of Battery; No Display/Image; Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Material Integrity Problem; Patient Device Interaction Problem; Premature Discharge of Battery; No Display/Image; Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Material Integrity Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEIR INSULIN PUMP HAD BUTTONS HARDER TO PRESSED MORE THAN ONCE. THE CUSTOMER¿S BLOOD GLUCOSE WAS 70 MG/DL TO 120 MG/DL AT THE TIME OF INCIDENT. CUSTOMER REPORTED THAT THE INSULIN PUMP HAD BATTERIES CHANGED FREQUENTLY EVERY THREE WEEKS, NO DELIVERY ALARM, HAD SHUT OFF ITS OWN, CHIPPED IN CASE THE AREA WHERE PUT THE BATTERY AND LOST BASAL SETTING. CUSTOMER REPORTED THAT THE INSULIN PUMP WAS NOT WORKING AND IT WAS NOT THE BATTERY IT WAS GOOD TOOK THE BATTERY OUT AND BACK IN AND IT STARTED WORKING AGAIN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8783713 ↗
• InjuryJul 2, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  CUSTOMER CALLED AND REPORTED THAT THEY GOT HOSPITALIZED DUE TO LOW BLOOD GLUCOSE WITH UNKNOWN BLOOD GLUCOSE LEVELS AT THE TIME OF THE INCIDENT. THE CUSTOMER DID NOT MENTION HOW THEY WERE TREATED. THE CUSTOMER DID NOT MENTION ANY SYMPTOMS. THE CUSTOMER WAS WEARING THE INSULIN PUMP DURING THE INCIDENT. TROUBLESHOOTING WAS NOT COMPLETED AS THE CUSTOMER DECLINED. THE CUSTOMER ALSO MENTIONED GETTING A HIGH. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS. FRN-UNK-RSVR . UNOMED SET.

  Patient problems: Hyperglycemia; Hypoglycemia

  MAUDE report 8752051 ↗
• MalfunctionJun 28, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE DRIVE SUPPORT CAP WAS DAMAGED. THE CUSTOMER'S BLOOD GLUCOSE VALUE WAS 90 MG/DL. CUSTOMER WAS ADVISED THE INSULIN PUMP WILL NEED TO BE REPLACED. ADVISED 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 8743228 ↗
• MalfunctionMay 1, 2019Device Displays Incorrect Message

  THE CUSTOMER¿S PARENT REPORTED VIA PHONE CALL THE INSULIN PUMP ALARMED BUTTON ERROR. THE CUSTOMER¿S BLOOD GLUCOSE WAS 295 MG/DL AT THE TIME OF INCIDENT. CUSTOMER¿S PARENT STATED THAT INSULIN PUMP ALARMED BUTTON ERROR AND THE ACT BUTTON WAS STUCK. NO SIGNIFICANT EVENTS LEADING TO BUTTON ERROR WERE OBSERVED. BUTTON ERROR TROUBLESHOOTING WAS PERFORMED AND UNABLE TO CONFIRM IF THE TIME IS ADVANCING DUE TO BATTERY HAS ALREADY BEEN REMOVED. THE CUSTOMER¿S PARENT WAS ADVISED TO HAVE THE CUSTOMER DISCONTINUE USE OF PUMP AND REVERT TO BACK-UP PLAN. THE INSULIN PUMP IS BEING REPLACED AND IS EXPECTED TO RETURN FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 8568054 ↗
• MalfunctionApr 22, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Battery Problem; Power Problem; Patient Device Interaction Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Battery Problem; Power Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEIR INSULIN PUMP WAS DAMAGED. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER REPORTED SCRATCHES ON DISPLAY SCREEN AND HARD TO SEE AND A BATTERY MAY LAST LESS THAN A WEEK SOMETIMES IT DOES SEEM TO TAKE A LITTLE LONGER TO REWIND. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND TO REVERT TO THE BACK-UP PLAN. THE DEVICE WAS NOT EXPECTED TO BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8534633 ↗
• MalfunctionMar 27, 2019Display or Visual Feedback Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Communication or Transmission Problem; Power Problem; Patient Device Interaction Problem; Display or Visual Feedback Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Communication or Transmission Problem; Power Problem; Patient Device Interaction Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD KEYPAD UNRESPONSIVE. THE CUSTOMER BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER STATED THAT THE UP AND DOWN ARROW WAS HARD TO PRESS MULTIPLE TIMES. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8455804 ↗
• InjuryMar 3, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE LEVEL. CUSTOMER'S BLOOD GLUCOSE VALUE WAS 300 MG/DL AT THE TIME OF THE INCIDENT AND 400 MG/DL. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING AND DECLINED FOR HIGH BLOOD GLUCOSE. THE CUSTOMER WAS TREATED WITH INSULIN PUMP. CUSTOMER WILL NOT BE RETURNED DEVICE FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 8385032 ↗
• MalfunctionFeb 5, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THE INSULIN PUMP ALARMED MOTOR ERROR AND A MOTOR POSITION ENCODER ERROR IN ALARM HISTORY. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 253 MG/DL. THE CUSTOMER STATED THAT THE DRIVE SUPPORT CAP WAS NORMAL. THE CUSTOMER STATED THAT THE INSULIN PUMP WAS NOT EXPOSED TO HIGH MAGNETIC FIELDS. CUSTOMER WAS ABLE TO SUCCESSFULLY CLEAR THE ALARM. 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: No Consequences Or Impact To Patient

  MAUDE report 8305167 ↗
• MalfunctionJan 4, 2019Patient Device Interaction Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THERE WAS A CRACK NEAR BATTERY COMPARTMENT. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 167 MG/DL. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8216474 ↗
• InjuryNov 7, 2018No Display/Image; Device Difficult to Program or Calibrate; Power Problem; No Display/Image; Device Difficult to Program or Calibrate; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEIR INSULIN PUMP HAD BATTERY OUT LIMIT ALARM. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS OVER 300 MG/DL AND THEY CORRECTED IT WITH MANUAL INJECTIONS. CUSTOMER REPORTED THAT THEY WERE UNABLE TO CLEAR THE BATTERY OUT LIMIT ALARM. CUSTOMER ALSO REPORTED THAT THE INSULIN PUMP HAD FAILED BATTERY ALERT AND WHEN THEY CHANGED THE BATTERY THE INSULIN PUMP DID NOT TURNED ON AGAIN. TROUBLESHOOTING WAS PERFORMED AND DISPLAY DID RETURNED. CUSTOMER REPORTED THAT THE TIME WAS ADVANCED. CUSTOMER REPORTED THAT THE INSULIN PUMP HAD FROZEN DISPLAY. 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 8049629 ↗
• MalfunctionOct 25, 2018Power Problem; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD BATTERY FAILED TEST ALARM. THE CUSTOMER BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER WAS NOT ASSISTED WITH TROUBLESHOOTING. CUSTOMER STATED THAT THE INSULIN PUMP REJECTED BATTERIES RECENTLY FIVE TO SIX TIMES. CUSTOMER HAD TO TAKE OUT AND REPLACE TO GET IT TO WORK NOT EFFECTING THE INSULIN PUMP. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8007781 ↗
• MalfunctionOct 22, 2018Power Problem; Power Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP REJECTS BATTERIES. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER ALSO REPORTED THAT THE INSULIN WAS SQUIRTING DURING MANUAL PRIME PROCESS. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7993411 ↗
• MalfunctionOct 1, 2018Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD KEYPAD ANOMALY, AUDIO ANOMALY AND REWIND ANOMALY. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER REPORTED THAT DURING REWIND THEY HAD LOUDER MADE A ¿STRUGGLING¿ SOUND AND INSULIN PUMP ALARM VOLUME WAS DECREASED, BATTERY LIFE DIMINISHED. IT WAS REPORTED THAT THEY HAD LIGHT SCRATCHES ON SCREEN AND ACT BUTTON WAS HARDER TO PRESS. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7924182 ↗

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-1587-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-522
• Z-1594-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723
• 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-1591-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523
• Z-1593-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723K
• 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-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