Paradigm® REAL-Time Revel™ MMT-723NAB (UDI 00643169077690)Recalls & reported problems

Summary

The FDA's MAUDE database contains 114 adverse event reports that list this exact device (DI 00643169077690), received between May 31, 2017 and Sep 25, 2020 — classified as 25 injuries, 89 malfunctions.

The most frequently reported specific device problem is “Device Displays Incorrect Message” (25 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 114 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 25, 2020Obstruction of Flow; Battery Problem; Obstruction of Flow; Battery Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD UNEXPECTED NO DELIVERY ALARMS. CUSTOMER STATED THAT BATTERY SETTINGS DID NOT REPOPULATED WHILE CHANGING 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 10589978 ↗
• MalfunctionAug 31, 2020Mechanical Problem; Obstruction of Flow; Material Integrity Problem; No Apparent Adverse Event; Mechanical Problem; Obstruction of Flow; Material Integrity Problem; No Apparent Adverse Event

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR. CUSTOMER STATED THAT THE INSULIN PUMP HAD A STRIPPED BATTERY CAP, SLOWER TO REWOUND AND UNEXPLAINED NO DELIVERY ALARM. 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 10475342 ↗
• InjuryJul 23, 2020Mechanical Problem; Obstruction of Flow; No Apparent Adverse Event; Mechanical Problem; Obstruction of Flow; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 400 MG/DL WHICH WAS TREATED WITH MANUAL INJECTION. CUSTOMER STATED THAT INSULIN PUMP HAD MOTOR ERROR AND NO DELIVERY ALARM. CUSTOMER STATED THAT DRIVE SUPPORT CAP WAS NORMAL. CUSTOMER DID NOT REPORT MOTOR POSITION ENCODER ERROR ALARM. CUSTOMER WAS ABLE TO CLEAR ALARM BUT PUT THE RESERVOIR IN THE INSULIN PUMP AGAIN AND THEN AN HOUR GOT ALARM AGAIN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 10313289 ↗
• MalfunctionJul 22, 2020Mechanical Problem; Obstruction of Flow; Mechanical Problem; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR. CUSTOMER CLEARED THE ALARM AND PUT THE RESERVOIR IN THE INSULIN PUMP AGAIN AND THEN AN HOUR GOT ALARM AGAIN. CUSTOMER REPORTED THE DRIVE SUPPORT CAP APPEARS NORMAL. 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 10306675 ↗
• MalfunctionJun 24, 2020No Display/Image; Battery Problem; Material Integrity Problem; Patient Device Interaction Problem; No Display/Image; Battery Problem; Material Integrity Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD ISSUES WITH BATTERY DRAINING FASTER. THE CUSTOMER STATED THAT THE INSULIN PUMP HAD BLANK DISPLAY. THE CUSTOMER STATED THAT THE INSULIN PUMP HAD CRACKED AT BATTERY COMPARTMENT. 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 10188186 ↗
• MalfunctionJun 15, 2020Failure to Cycle; Priming Problem; Failure to Cycle; Priming Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP HAD COMPROMISED FORCE SENSOR SYSTEM ALARM AND JUST SHOOTS THE INSULIN OUT OF THE RESERVOIR. CUSTOMER WERE UNABLE TO CLEAR THE ALARM AND ALSO WERE UNABLE TO REWIND THE 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 10152078 ↗
• MalfunctionApr 23, 2020Failure to Cycle; Mechanical Problem; Failure to Cycle; Mechanical Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A COMPROMISED FORCE SENSOR SYSTEM ALARM. THE CUSTOMER STATED THE INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER REPORTED THEY WERE ABLE TO CLEAR THE ALARM. CUSTOMER WAS NOT ABLE TO COMPLETE REWIND. 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 9989377 ↗
• MalfunctionApr 21, 2020Mechanical Problem; Moisture or Humidity Problem; Mechanical Problem; Moisture or Humidity Problem

  CUSTOMER REPORTED VIA PHONE CALL THE INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER BLOOD GLUCOSE AT THE TIME OF INCIDENT WAS UNKNOWN. THE INSULIN WAS EXPOSED TO MOISTURE. TROUBLESHOOTING WAS NOT PERFORMED. THE INSULIN PUMP WILL NOT BE RETURNING FOR ANALYSIS

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9984022 ↗
• MalfunctionApr 7, 2020Mechanical Problem; Obstruction of Flow; Mechanical Problem; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR. CUSTOMER WAS ABLE TO CLEAR THE ALARM. CUSTOMER REPORTED THAT THEY RECEIVED INSULIN PUMP'S HISTORY HAD MOTOR POSITION ENCODER ERROR. CUSTOMER REPORTED THAT THE DRIVE SUPPORT CAP WAS NORMAL. CUSTOMER WAS ABLE TO REWIND THE INSULIN PUMP. INSULIN PUMP ALSO HAD INSULIN FLOW BLOCK ALARM. 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 9932407 ↗
• MalfunctionApr 2, 2020Moisture or Humidity Problem; Patient Device Interaction Problem; Moisture or Humidity Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP¿S SCRATCHES IN THE SCREEN MAKE IT DIFFICULT TO READ THE SCREEN AND THE CORROSION IN THE BATTERY CHAMBER MAKES ME SUSPICIOUS THAT MOISTURE HAS LEAKED IN TO IT. 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 9917804 ↗
• MalfunctionMar 26, 2020Failure to Cycle; Mechanical Problem; Detachment of Device or Device Component; Failure to Cycle; Mechanical Problem; Detachment of Device or Device Component

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A COMPROMISED FORCE SENSOR SYSTEM ALARM AND MOTOR ERROR. THE CUSTOMER STATED THE DEVICE WAS SQUIRTING INSULIN OUT DURING MANUAL PRIME PROCESS. THE DEVICE 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 9881972 ↗
• MalfunctionMar 8, 2020Patient Device Interaction Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP WAS NOT WORKING. THE CUSTOMER STATED THAT THERE WAS CRACKED ON THE THREADING OF THE BATTERY CAP AREA. CUSTOMER STATED THE INSULIN PUMP HAD COSMETIC DAMAGE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WAS RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9804009 ↗
• MalfunctionMar 6, 2020Device Difficult to Program or Calibrate; Moisture or Humidity Problem; Patient Device Interaction Problem; Device Difficult to Program or Calibrate; Moisture or Humidity Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE BUTTON OF THE INSULIN PUMP WAS NOT WORKING. THE INSULIN PUMP WAS NO LONGER WATER PROOF. CUSTOMER REPORTED THAT THE KEYPAD WAS FOGGED UP. BATTERY COMPARTMENT OF THE INSULIN PUMP WAS DAMAGED. CUSTOMER DID NOT MENTIONED DAMAGED TO THE RESERVOIR LIP RING. CUSTOMER DECLINED TO CONTINUE THE INSULIN PUMP TROUBLESHOOTING. 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 9797035 ↗
• MalfunctionJan 8, 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 A COMPROMISED FORCE SENSOR SYSTEM ALARM AND THE DRIVE SUPPORT CAP WAS STICKING OUT. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE INSULIN PUMP WAS NOT WORKING CORRECTLY. 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 9567291 ↗
• MalfunctionDec 23, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE BUTTONS WERE STICKING AND WERE NOT RESPONSIVE ANYMORE. 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 9510234 ↗
• MalfunctionDec 11, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP BOLUS BUTTON STOPPED WORKING AND THE INSULIN PUMP ALARMED WITH BUTTON ERROR AND NOTHING WORKS. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 200 MG/DL. CUSTOMER STATED TIME DID NOT ADVANCED. TROUBLESHOOTING WAS PERFORMED. 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 PER HEALTH CARE PROFESSIONAL INSTRUCTIONS. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9449101 ↗
• MalfunctionDec 6, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Power Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE BUTTONS WERE HARDER TO PRESS AND BATTERY LIFE WAS DIMINISHED AND PLASTIC PIECE GET PUSHED OUT. 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 9422463 ↗
• MalfunctionNov 7, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP WAS NOT ALLOWING HIM TO GO DOWN ONLY UPWARD WHEN HE ENTERED A BLOOD GLUCOSE VALUE AND IT SCROLLED ON ITS OWN. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 140 MG/DL. THE CUSTOMER MENTIONED THAT ALL THE KEYS HAD STOPPED RESPONDING. THE CUSTOMER STATED THAT THE TIME ON THE INSULIN PUMP WAS ADVANCING. CUSTOMER WAS ADVISED THAT THE INSULIN PUMP WILL NEED TO BE REPLACED. THE CUSTOMER WAS ADVISED TO DISCONNECT FROM THE INSULIN PUMP AND REVERT TO THE BACKUP PLAN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9289045 ↗
• MalfunctionOct 16, 2019Mechanical Problem; Obstruction of Flow; Power Problem; Patient Device Interaction Problem; Mechanical Problem; Obstruction of Flow; Power Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEIR INSULIN PUMP HAD SCRATCH ON THE SCREEN AND HARD TO READ THE SCREEN, ACT BUTTON WAS WORN OFF, MOTOR ERROR AND RESERVOIR WAS NOT LOCK IN PLACE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. INSULIN PUMP HAD REJECTED BATTERIES. CUSTOMER DOES NOT WANT TO TROUBLESHOOTING FOR KEYPAD ANOMALY, NO DELIVERY ALARM, BATTERY ISSUES. CUSTOMER WAS REPORTING PAST EVENT. 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 9196580 ↗
• MalfunctionOct 1, 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 A BLACK DOT INSIDE A CIRCLE ON THE INSULIN PUMP SCREEN. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER REPORTED THAT THE BATTERY COMPARTMENT AND BROKEN CLIP RAILS HAS A CRACK ON IT. CUSTOMER WAS ADVISED THAT THE INSULIN PUMP WILL NEED TO BE REPLACED. THE CUSTOMER WAS ADVISED TO DISCONNECT FROM THE INSULIN PUMP AND REVERT TO THE BACKUP PLAN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9138232 ↗
• MalfunctionSep 3, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE BUTTON KEYPAD WAS NOT RESPONDING OF INSULIN PUMP. THE CUSTOMER'S BLOOD GLUCOSE VALUE WAS 150 MG/DL AT THE TIME OF INCIDENT. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8954801 ↗
• MalfunctionSep 2, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER REPORTED VIA PHONE CALL THAT DRIVE SUPPORT CAP WAS DAMAGED. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 140 MG/DL AT THE TIME OF INCIDENT. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8953229 ↗
• MalfunctionAug 20, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD KEYPAD ANOMALY. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 119 MG/DL. CUSTOMER STATED THAT NONE OF THE BUTTONS WERE RESPONDING. CUSTOMER WAS ADVISED THAT THE INSULIN PUMP WILL NEED TO BE REPLACED. CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND REVERT TO BACKUP PLAN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8909612 ↗
• InjuryAug 20, 2019Mechanical Problem; Obstruction of Flow; Detachment of Device or Device Component; Mechanical Problem; Obstruction of Flow; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE CUSTOMER RECEIVED EMERGENCY MEDICAL ASSISTANCE DUE TO LOW BLOOD GLUCOSE 2 MONTHS PREVIOUSLY WITH BLOOD GLUCOSE OF 27 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER WAS FOUND ON THE SIDE OF THE ROAD IN THEIR CAR WITH THE HAZARD LIGHTS ON. THE REPORTING PARTY DID NOT MENTION HOW THE CUSTOMER WAS TREATED. THE REPORTING PARTY DID NOT MENTION ANY SYMPTOMS. THE CUSTOMER WAS WEARING THE INSULIN PUMP DURING THE INCIDENT. THE CUSTOMER EMAILED THAT THE PUMP'S DRIVE SUPPORT CAP WAS PROTRUDED, AND THEY WERE GETTING NO DELIVERY ALARMS AS WELL AS A MOTOR ERROR ALARM. THE CUSTOMER MENTIONED OUT OF CONTROL BLOOD GLUCOSE LEVELS. TROUBLESHOOTING WAS NOT COMPLETED AS THE CUSTOMER COULD NOT BE REACHED. THE CUSTOMER USES A COMPETITOR'S SENSOR SYSTEM. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia; Hypoglycemia

  MAUDE report 8909252 ↗
• MalfunctionAug 5, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM. THE CUSTOMER BLOOD GLUCOSE LEVEL WAS 230 MG/DL. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. CUSTOMER REPORTED THAT THEY WERE ABLE TO CLEAR THE ALARM AND UNABLE TO COMPLETE REWIND. CUSTOMER STATED THAT DRIVE SUPPORT CAP APPEARS TO BE NORMAL. 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 PER HEALTH CARE PROFESSIONAL INSTRUCTIONS. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8858813 ↗

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-1593-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723K
• 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-1587-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-522
• Z-1591-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523
• Z-1589-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-522K
• 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-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