Paradigm® REAL-Time Revel™ MMT-723LNAP (UDI 00643169933163)Recalls & reported problems

Summary

The FDA's MAUDE database contains 107 adverse event reports that list this exact device (DI 00643169933163), received between Jan 8, 2018 and Jul 22, 2020 — classified as 1 death, 44 injuries, 62 malfunctions.

The most frequently reported specific device problem is “Device Difficult to Program or Calibrate” (25 reports).

14 other recalls cover devices cleared under the same FDA submission (P150019, 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 107 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 22, 2020Device Alarm System; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Material Integrity Problem; Device Alarm System; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Material Integrity Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP HAD BUTTONS ARE HARDER TO PUSHED, ALARM WAS NOT AS LOUD AS IT USED TO BE AND RECEIVED NO DELIVERY ALARM. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER STATED THAT INSULIN PUMP REJECTED NEW BATTERY AND REWIND WAS SLOWER. THE BATTERY CAP WAS HARD TO GET TIGHTENED ALL THE WAY DOWN. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10306669 ↗
• MalfunctionJul 21, 2020Premature Discharge of Battery; Battery Problem; Loss of Data; Premature Discharge of Battery; Battery Problem; Loss of Data

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD LOW BATTERY ALARMS, OFF NO POWER AND MULTIPLE INSULIN PUMP ERROR. THE CUSTOMER WAS ABLE TO CLEAR THE ALARM AND ABLE TO REWIND THE INSULIN PUMP. THE INSULIN PUMP ALARM SHORTLY AFTER INSERTING A NEW BATTERY. 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 10302011 ↗
• MalfunctionJun 8, 2020Failure to Cycle; Failure to Cycle

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A COMPROMISED FORCED SENSOR SYSTEM ERROR ALARM. THE CUSTOMER REPORTED THAT THEY HAD TAKEN THE INSULIN PUMP OFF TO JUMP ON THE TRAMPOLINE, THEN HAD PUT THE INSULIN PUMP BACK ON AND THEN IT JUST STARTED FLASHING NUMBERS AND RESTARTED AND CAME UP WITH AN ERROR. THE DRIVE SUPPORT CAP APPEARED NORMAL. THE CUSTOMER ALSO REPORTED THAT HIS BELT CLIP WAS DIRTY AND REQUESTED FOR A NEW ONE. 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 10128894 ↗
• MalfunctionMay 14, 2020Failure to Cycle; Failure to Cycle

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A COMPROMISED FORCED SENSOR SYSTEM ERROR ALARM. THE CUSTOMER REPORTED THAT THEY HAD TAKEN THE INSULIN PUMP OFF TO JUMP ON THE TRAMPOLINE, THEN HAD PUT THE INSULIN PUMP BACK ON AND THEN IT JUST STARTED FLASHING NUMBERS AND RESTARTED AND CAME UP WITH AN ERROR. THE DRIVE SUPPORT CAP APPEARED NORMAL. THE CUSTOMER ALSO REPORTED THAT HIS BELT CLIP WAS DIRTY AND REQUESTED FOR A NEW ONE. 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 10054743 ↗
• MalfunctionApr 16, 2020Mechanical Problem; Adverse Event Without Identified Device or Use Problem; Mechanical Problem; Adverse Event Without Identified Device or Use Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9966993 ↗
• MalfunctionApr 7, 2020Mechanical Problem; Device Difficult to Program or Calibrate; Mechanical Problem; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE BUTTONS WERE NEED TO PRESS MORE TO RESPOND. INSULIN PUMP MADE GRINDING NOISE DURING REWIND. 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 9933505 ↗
• MalfunctionMar 31, 2020Premature Discharge of Battery; Premature Discharge of Battery

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY HAD AN INSULIN PUMP ERROR. THE CUSTOMER'S BLOOD GLUCOSE LEVELS WERE UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER STATES THEY HAVE HAD ISSUES FOR LAST 6 MONTHS. TROUBLESHOOTING WAS PERFORMED HOWEVER THE INSULIN PUMP ERROR HAPPENED AGAIN. THE INSULIN PUMP IS RETURNING FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9902210 ↗
• MalfunctionMar 20, 2020Mechanical Problem; Mechanical Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR. CUSTOMER STATED THAT DRIVE SUPPORT CAP WAS NORMAL. CUSTOMER STATES PUMP WAS NOT EXPOSED TO A HIGH MAGNETIC FIELD. CUSTOMER WAS ABLE TO CLEAR THE ALARM BUT UNABLE TO REWIND THE PUMP. CUSTOMER WAS UNABLE TO DESCRIBE DAMAGE TO DRIVE SUPPORT CAP. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9859246 ↗
• MalfunctionMar 11, 2020Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE ACT BUTTONS WAS NOT RESPONSIVE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia; Hypoglycemia

  MAUDE report 9816487 ↗
• MalfunctionFeb 28, 2020Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP'S ACT BUTTON WAS NOT RESPONDING. THE CUSTOMER STATED INSULIN PUMP'S TIME ADVANCED. 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 9767960 ↗
• MalfunctionFeb 26, 2020Mechanical Problem; Detachment of Device or Device Component; Mechanical Problem; Detachment of Device or Device Component

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR DURING REWIND AND ALSO RECEIVED NO DELIVERY ALARM WHICH WAS RESOLVED BY COMPLETE SET CHANGE. CUSTOMER REPORTED THAT THE TROUBLESHOOTING WAS PERFORMED. INSULIN PUMP WAS UNABLE TO REWIND. THE DRIVE SUPPORT CAP WAS FLUSHED. 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 9754736 ↗
• MalfunctionFeb 10, 2020Device Alarm System; Mechanical Problem; Device Difficult to Program or Calibrate; Power Problem; Device Alarm System; Mechanical Problem; Device Difficult to Program or Calibrate; Power Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD BUTTON ERRORS, STICKY NON-RESPONSIVE BUTTONS AND IT DID NOT WORKED. CUSTOMER ALSO REPORTED SUDDEN POWER DOWN- NO BATTERY WARNING, GRINDING DURING THE REWIND PROCESS, REJECTED NEW BATTERIES, CRACKED SCREEN AND TEMPORARY LOST SETTINGS. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9685361 ↗
• MalfunctionFeb 7, 2020Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP BUTTONS WERE RANDOMLY RESPONDING AND KEYPAD WAS UNRESPONSIVE. TROUBLESHOOTING WAS PERFORMED FOR KEYPAD ANOMALY. 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 9681191 ↗
• InjuryFeb 3, 2020Material Integrity Problem; No Apparent Adverse Event; Material Integrity Problem; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 459 MG/DL. CUSTOMER STATED THAT BATTERY CAP WAS DAMAGED. CUSTOMER ATTRIBUTED THE HIGH BLOOD GLUCOSE TO A TOOTH INFECTION. CUSTOMER WAS DECLINED TO TROUBLESHOOT FOR HIGH BLOOD GLUCOSE. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9658633 ↗
• DeathFeb 3, 2020Adverse 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 HOSPITAL ON (B)(6) 2019. THE CUSTOMER WAS HOSPITALIZED THREE WEEKS PRIOR DUE TO A LOW BLOOD GLUCOSE. THE CAUSE OF DEATH WAS REPORTED AS MULTIPLE REASONS RELATED TO LOW BLOOD GLUCOSE. THE CUSTOMER'S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF DEATH. THE CALLER STATED THAT THE CUSTOMER ACCIDENTALLY DELIVERED TOO MUCH INSULIN. THE CUSTOMER RAN OUT OF INSULIN DURING AN INITIAL BOLUS, FILLED A NEW RESERVOIR, AND ADMINISTERED A SECONDARY BOLUS WHICH RESULTED IN THEM DELIVERING TOO MUCH INSULIN. THE CUSTOMER EXPERIENCED A LOW BLOOD GLUCOSE AND BECAME SEMI-UNCONSCIOUS WHICH IS WHEN THE FAMILY CALLED EMERGENCY MEDICAL SERVICES. THE CALLER STATED THE CUSTOMER SPENT THREE WEEKS AT THE HOSPITAL IN CRITICAL CARE AND THEN PASSED AWAY DUE TO INCORRECT ACTIONS TAKEN BY THE HOSPITAL. THE CALLER STATED THE CUSTOMER DID NOT EXPERIENCE A MALFUNCTION WITH THEIR INSULIN PUMP LEADING UP TO THE PASSING. THE INSULIN PUMP WAS NOT WORN AT THE TIME OF PASSING AND WAS REMOVED BY HOSPITAL STAFF UPON ADMISSION THREE WEEKS PRIOR. THE CUSTOMER WAS NOT USING SENSORS. THE CALLER DECLINED TO RETURN THE INSULIN PUMP AS THEY DID NOT HAVE THE DEVICE.

  Patient problems: Death; Hypoglycemia; Loss of consciousness

  MAUDE report 9658612 ↗
• MalfunctionJan 9, 2020Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE BUTTONS WERE STIFF. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9568242 ↗
• MalfunctionJan 9, 2020Connection Problem; Patient Device Interaction Problem; Connection Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT RESERVOIR LIP RING WAS DAMAGED. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER REPORTED THAT THE INSULIN PUMP HAD CRACKS AROUND THE RESERVOIR COMPARTMENT AND THAT WHERE THE RESERVOIR LOCKS INTO THE PUMP HAS BROKEN OFF. CUSTOMER STATED THAT RESERVOIR WAS UNABLE TO LOCK IN PLACE WHEN INSERTED INTO INSULIN PUMP. 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 9567709 ↗
• MalfunctionDec 17, 2019Mechanical Problem; Patient Device Interaction Problem; Mechanical Problem; Patient Device Interaction Problem

  IT WAS REPORTED THAT THE INSULIN PUMP HAD MOTOR ERROR. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF INCIDENT. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. IT WAS REPORTED THAT MOTOR ERROR WAS OCCURRED FEW DAYS AGO. DOME LABEL STICKER ON THE END OF WAS NOT PRESENT ON THE INSULIN PUMP. 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 9480414 ↗
• MalfunctionDec 10, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP BUTTON GOT STUCK AND CANNOT REWIND THE INSULIN PUMP. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER REPORTED THAT THE REWIND INSULIN PUMP AND THEN ISSUE OCCURRED. CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE DEVICE 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 9443316 ↗
• MalfunctionNov 28, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Use of Device Problem; Obstruction of Flow; Mechanical Problem; Device Difficult to Program or Calibrate; Use of Device Problem; Obstruction of Flow

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD BUTTONS HARDER TO PRESS AND HAD TO PRESS MULTIPLE TIMES. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF INCIDENT. THE CUSTOMER ALSO STATED THAT INSULIN PUMP HAD LOST SETTINGS DURING BATTERY CHANGE, DATE AND TIME RESETS WITH BATTERY CHANGE, REWIND TAKES LONGER AND INSULIN PUMP RECEIVES RANDOM NO DELIVERY ALERTS. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9388371 ↗
• MalfunctionNov 18, 2019Device Alarm System; Device Difficult to Program or Calibrate; Device Alarm System; Device Difficult to Program or Calibrate

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP¿S BUTTONS WERE HARDER TO PRESS AND RESPONSE. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER ALSO STATED THAT THE INSULIN PUMP DID NOT RECEIVED INSULIN FLOW BLOCKED ALARM EVEN AFTER CANNULA WAS KINKED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9333781 ↗
• MalfunctionNov 17, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER;S TERRITORY MANAGER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP KEYS WERE NOT RESPONDING PROPERLY AND MAINLY THE ACT KEY BUT ALL OF THEM WERE NOT RESPONDING. CUSTOMER'S BLOOD GLUCOSE VALUE WAS UNKNOWN. TROUBLESHOOTING WAS PERFORMED. CUSTOMER STATED THAT THE TIME CLOCK FOR ONE MINUTE WAS ADVANCES. 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 9333704 ↗
• MalfunctionOct 29, 2019Device Difficult to Program or Calibrate; Obstruction of Flow; Device Difficult to Program or Calibrate; Obstruction of Flow

  CUSTOMER REPORTED VIA PHONE CALL THAT THE BUTTONS ARE HARDER TO PRESS. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF INCIDENT. CUSTOMER STATED THAT INSULIN PUMP HAD UNEXPLAINED NO DELIVERY ALERTS NOT DUE TO SITE ISSUES. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9248508 ↗
• MalfunctionOct 18, 2019Connection Problem; Material Integrity Problem; Patient Device Interaction Problem; Connection Problem; Material Integrity Problem; Patient Device Interaction Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT RESERVOIR WAS NOT ABLE TO LOCK IN PLACE WHEN INSERTED INTO INSULIN PUMP. CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN. CUSTOMER STATED THAT THREADING WERE MESSING UP ON RESERVOIR COMPARTMENT. CUSTOMER MENTIONED THAT SOMETIMES RESERVOIR WILL LOCK IN PLACE AND SOMETIMES WILL NOT LOCK. CUSTOMER STATED THAT RUBBER PIECE FELL OFF FROM THE BATTERY CAP. CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE PUMP AND REVERT TO BACKUP PLAN. INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9206373 ↗
• MalfunctionSep 9, 2019Device Alarm System; Device Difficult to Program or Calibrate; Battery Problem; Power Problem; Device Alarm System; Device Difficult to Program or Calibrate; Battery Problem; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP'S BUTTONS DID NOT RESPOND ALWAYS AND INSULIN PUMP REJECTING THE NEW BATTERIES. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER STATED THAT THE INSULIN PUMP NOT GAVE ANY ALARM WHEN THE INSULIN WAS NOT DELIVERED. CUSTOMER REPORTED THAT THE BATTERY LIFE WAS DIMINISHED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8974154 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P150019, 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-1589-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-522K
• 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-1588-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-722
• Z-1592-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523K
• Z-1590-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-722K
• 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