Paradigm® REAL-Time Revel™ MMT-723NAP (UDI 00643169446465)Recalls & reported problems

Summary

The FDA's MAUDE database contains 273 adverse event reports that list this exact device (DI 00643169446465), received between May 3, 2017 and Aug 3, 2020 — classified as 74 injuries, 199 malfunctions.

The most frequently reported specific device problem is “Device Displays Incorrect Message” (54 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 273 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 3, 2020Failure to Cycle; Failure to Cycle

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD COMPROMISED FORCE SENSOR SYSTEM ALARM. CUSTOMER STATED DRIVE SUPPORT CAP APPEARS NORMAL. TROUBLESHOOTING WAS PERFORMED. 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 10355071 ↗
• MalfunctionJul 14, 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 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 10270206 ↗
• MalfunctionJun 17, 2020No Display/Image; No Display/Image

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP WAS NOT STARTING. CUSTOMER CHANGED THE BATTERY AND CLEANED OUT THE BATTERY CHAMBER BUT STILL NOTHING HAPPENED. 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 10161614 ↗
• MalfunctionMay 27, 2020Insufficient Flow or Under Infusion; Insufficient Flow or Under Infusion

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP DID NOT BOLUS 3 TO 4 TIMES IN THE LAST WEEK. 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 10091199 ↗
• MalfunctionApr 6, 2020Obstruction of Flow; Material Integrity Problem; Obstruction of Flow; Material Integrity Problem

  THE CUSTOMER REPORTED THAT THEY RECEIVED NO DELIVERY ALARM IN THE ALARM HISTORY. THE CUSTOMER'S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF INCIDENT. THE CUSTOMER ALSO BATTERY CAP ISSUES. TROUBLESHOOTING WAS NOT PROVIDED. NO OTHER INFORMATION WAS GIVEN. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9927766 ↗
• MalfunctionApr 2, 2020Display or Visual Feedback Problem; Mechanical Problem; Obstruction of Flow; Priming Problem; Display or Visual Feedback Problem; Mechanical Problem; Obstruction of Flow; Priming Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP SQUIRTING OUT THE INSULIN INSTEAD OF NORMAL DROPLET DELIVERY. INSULIN PUMP LOUDER DURING REWOUND AND HAD UNEXPLAINED NO DELIVERY ALARMS. 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 9915483 ↗
• MalfunctionMar 19, 2020Computer Software Problem; Mechanical Problem; Patient Device Interaction Problem; Computer Software Problem; Mechanical Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD UNSPECIFIED ALARM AND REWIND WAS LOUDER AND PIECE CHIPPED OFF. 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 9852610 ↗
• MalfunctionFeb 10, 2020No Display/Image; Patient Device Interaction Problem; No Display/Image; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A BLANK DISPLAY. CUSTOMER STATED THE BATTERY WAS CHANGED MULTIPLE TIMES, BUT THE ISSUE WAS NOT RESOLVED. CUSTOMER STATED THAT SHE CHANGED THE BATTERY AND THE SPRING INSIDE THE PUMP CAME 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 9685718 ↗
• MalfunctionJan 17, 2020Mechanical Problem; Device Difficult to Program or Calibrate; Battery Problem; Power Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Battery Problem; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERRORS, BUTTONS WERE HARD TO PRESS AND INSULIN PUMP REJECTED NEW BATTERIES. CUSTOMER'S BLOOD GLUCOSE VALUE WAS UNKNOWN. CUSTOMER DECLINED TO REPORT TO 24 HOURS HELPLINE TECHNICAL SUPPORT DEPARTMENT. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9600174 ↗
• MalfunctionDec 30, 2019Display or Visual Feedback Problem; Obstruction of Flow; Power Problem; Insufficient Device Problem Information; Patient Device Interaction Problem; Display or Visual Feedback Problem; Obstruction of Flow; Power Problem; Insufficient Device Problem Information; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT INSULIN PUMP HAD RAINBOW EFFECT AND HARD TO READ. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER STATED THAT THEY RECEIVED UNEXPLAINED AND RANDOM NO DELIVERY ALARM. CUSTOMER STATED THAT THEY CHANGE THE BATTERY AND INSULIN PUMP REJECT THE NEW BATTERY. CUSTOMER STATED THAT INSULIN PUMP HAD SCRATCHES ON THE DISPLAY. CUSTOMER REPORTED THAT THEY CHANGE INFUSION AND ERROR STOPPED SOMETIMES. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9528883 ↗
• MalfunctionDec 23, 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 UNKNOWN. THE CUSTOMER REPORTED THAT THE UP BUTTON DOES NOT RESPOND. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9509482 ↗
• MalfunctionDec 10, 2019No Display/Image; No Display/Image

  CUSTOMER REPORTED VIA PHONE CALL THAT INSULIN PUMP STOPPED WORKING AND WENT BACK TO MULTI DOSE INJECTION. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF INCIDENT. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9443146 ↗
• MalfunctionNov 29, 2019Premature Discharge of Battery; Premature Discharge of Battery

  CUSTOMER REPORTED VIA PHONE CALL THAT INSULIN PUMP ALARMED FOR UNEXPECTED RESTART. CUSTOMER¿S BLOOD GLUCOSE WAS 103 MG/DL. CUSTOMER WAS NOT ABLE TO REWIND THE INSULIN PUMP. INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9391503 ↗
• MalfunctionNov 19, 2019Failure to Cycle; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Failure to Cycle; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow

  CUSTOMER REPORTED VIA PHONE CALL THAT INSULIN PUMP UP ARROW BUTTON HAD TO PRESS HARDER TO WORK AND INSULIN PUMP STOPS ON ITS OWN. CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF INCIDENT. THE CUSTOMER STATED THAT INSULIN PUMP HAD UNEXPLAINED NO DELIVERY ALARMS SEVERAL TIMES, MOTOR WAS SLOWER, LOUDER GRINDING DURING REWIND AND INSULIN SHOOTS UP DURING PRIMING. TROUBLESHOOTING WAS PERFORMED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9340472 ↗
• MalfunctionNov 16, 2019No Display/Image; No Display/Image

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD BLANK DISPLAY. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER STATED DISPLAY RETURNED AND SERIAL NUMBER WAS NO LONGER VISIBLE AND ITS PEELING OFF THEY TRIED ENTERING A NEW BATTERY 12 TIMES AND THE DISPLAY DID NOT CAME UP. 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 9332902 ↗
• MalfunctionNov 14, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Adverse Event Without Identified Device or Use Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD KEYPAD ANOMALY. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 200 MG/DL. THE CUSTOMER REPORTED THAT THE BUTTONS WERE STICKY ON UP AND DOWN BUTTONS, REWIND TOOK LONGER THAN BEFORE AND HAD RECEIVED UNEXPLAINED NO DELIVERY ALERTS. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE PUMP AND REVERT TO BACKUP PLAN PER HEALTH CARE PROFESSIONAL INSTRUCTIONS. THE CUSTOMER WAS ADVISED THE PUMP WILL NEED TO BE REPLACED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9320028 ↗
• MalfunctionNov 11, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP ESCAPE BUTTON HARD TO PRESS. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9304435 ↗
• MalfunctionNov 7, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEIR INSULIN PUMP HAD MOTOR ERROR ALARMED. THE CUSTOMER¿S BLOOD GLUCOSE WAS 220 MG/DL AT THE TIME OF INCIDENT. CUSTOMER REPORTED THAT THE DRIVE SUPPORT CAP APPEARS NORMAL. CUSTOMER DID NOT REPORTED MOTOR POSITION ENCODER ERROR ALARM. CUSTOMER WAS ABLE TO SUCCESSFULLY CLEAR THE ALARM. CUSTOMER WAS UNABLE TO COMPLETE INSULIN 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 AS PER HEALTH CARE PROFESSIONAL INSTRUCTION. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9290121 ↗
• InjuryNov 1, 2019Excess Flow or Over-Infusion; Excess Flow or Over-Infusion

  CUSTOMER CALLED AND REPORTED THAT THEY RECEIVED EMERGENCY MEDICAL ASSISTANCE DUE TO LOW BLOOD GLUCOSE ON (B)(6) 2019 WITH BLOOD GLUCOSE OF 44 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER DID NOT MENTION HOW THEY TREATED. THE CUSTOMER EXPERIENCED SYMPTOMS SUCH AS LOSS OF CONSCIOUSNESS. THE CUSTOMER WAS WEARING THE INSULIN PUMP DURING THE INCIDENT. THE CUSTOMER REPORTED A FLUSH PUMP DRIVE SUPPORT CAP AND BELIEVES THE PUMP IS OVER DELIVERING. TROUBLESHOOTING WAS COMPLETED BUT DID NOT RESOLVE THE ISSUE. THE CUSTOMER HAD A LOW BLOOD PRESSURE INCIDENT WHERE THEY FELL ON THEIR FACE, BUT DID NOT GET HOSPITALIZED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hypoglycemia; Loss of consciousness

  MAUDE report 9265152 ↗
• MalfunctionOct 29, 2019Mechanical Problem; Obstruction of Flow; Mechanical Problem; Obstruction of Flow

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR POSITION ENCODER ERROR ALARM AND MOTOR ERROR ALARM IN HISTORY. CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN. CUSTOMER STATED THAT DRIVE SUPPORT CAP WAS NORMAL. TROUBLESHOOTING WAS NOT PERFORMED DUE TO MOTOR ERROR. CUSTOMER WAS ABLE TO CLEAR THE ALARM AND ABLE TO COMPLETE INSULIN PUMP REWIND. TROUBLESHOOTING WAS DECLINED FOR HYPERGLYCEMIA. CUSTOMER ALSO REPORTED THAT THE INSULIN PUMP HAD NO DELIVERY ALARM. CUSTOMER WAS ADVISED TO THE INSULIN PUMP WOULD NEED TO BE REPLACED, TO DISCONTINUE USE OF THE INSULIN PUMP AND REFER TO BACK UP PLAN. INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9254075 ↗
• InjuryOct 23, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER'S WIFE REPORTED VIA PHONE CALL THAT CUSTOMER EXPERIENCED HYPERGLYCEMIA. THE CUSTOMER BLOOD GLUCOSE LEVELS WERE 450 MG/DL, 327 MG/DL, 300 MG/DL, 380 MG/DL, 100 MG/DL. THE CUSTOMER WAS TREATED WITH BOLUS FOR HIGH BLOOD GLUCOSE. CUSTOMER REPORTED THEY CONTACT THEIR HEALTH CARE PROFESSIONAL REGARDING THE HIGH BLOOD GLUCOSE. CUSTOMER WAS NEITHER IN EMERGENCY ROOM, NOR ADMITTED INTO HOSPITAL. CUSTOMER REPORTED THAT THE INSULIN PUMP WAS NOT ON AUTO MODE AT THE TIME OF INCIDENT. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9227482 ↗
• MalfunctionOct 23, 2019Premature Discharge of Battery; Battery Problem; Loss of Data; Power Problem; Premature Discharge of Battery; Battery Problem; Loss of Data; Power Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT INSULIN PUMP HAD UNEXPECTED RESTART AND POWER OFF. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER STATED THAT THEY WERE ABLE TO CLEAR THE ALARM AND ABLE TO COMPLETE REWIND BUT ALARM REOCCURRED AFTER BATTERY CHANGE. CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND REVERT TO BACK UP PLAN PER HEALTH CARE PROFESSIONAL. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9222642 ↗
• MalfunctionOct 16, 2019Display or Visual Feedback Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Display or Visual Feedback Problem; Device Difficult to Program or Calibrate; Obstruction of Flow

  CUSTOMER REPORTED VIA PHONE CALL THAT INSULIN PUMP ACT BUTTON WAS NON RESPONSIVE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER STATED INSULIN PUMP HAD NO DELIVERY ALARM AND BACK LIGHT WAS DIMMER. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9196506 ↗
• InjuryOct 15, 2019Insufficient Flow or Under Infusion; No Apparent Adverse Event; Insufficient Flow or Under Infusion; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE C ALL THAT THEY EXPERIENCED HYPERGLYCEMIA AND INSULIN PUMP WAS NOT DELIVERING INSULIN. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 400 MG/DL AND 323 MG/DL. THE CUSTOMER WAS TREATED WITH MANUAL SHOTS. CUSTOMER HAS BEEN USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE EVENT. THE CUSTOMER REPORTED THAT THE INSULIN PUMP WAS UNDER DELIVERING. CUSTOMER REPORTS INSULIN EXITED AT THE QUICK RELEASE. THE CUSTOMER REPORTED THAT THE SELF TEST PASSED. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9191077 ↗
• MalfunctionOct 11, 2019Device Difficult to Program or Calibrate; Battery Problem; Power Problem; Device Difficult to Program or Calibrate; Battery Problem; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD BUTTON ISSUES WHICH WERE STIFF. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER ALSO REPORTED CHANGING BATTERY MORE FREQUENTLY, DIMINISHED BATTERY LIFE AND INSULIN PUMP HAD REJECTED NEW BATTERY QUITE OFTEN. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9178230 ↗

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-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-1591-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523
• 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-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-1592-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523K
• 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