Paradigm® REAL-Time Revel™ MMT-723NAL (UDI 00643169446458)Recalls & reported problems

Summary

The FDA's MAUDE database contains 219 adverse event reports that list this exact device (DI 00643169446458), received between Jun 1, 2017 and Aug 14, 2020 — classified as 1 death, 52 injuries, 166 malfunctions.

The most frequently reported specific device problem is “Device Displays Incorrect Message” (42 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 219 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 14, 2020Failure to Cycle; Failure to Cycle

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A COMPROMISED FORCE SENSOR SYSTEM ALARM. CUSTOMER STATED THAT 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 10405878 ↗
• MalfunctionAug 6, 2020No Display/Image; No Display/Image

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THEY INSULIN PUMP HAD BLANK DISPLAY. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. CUSTOMER STATED THAT INSULIN PUMP WAS NOT EXPOSED TO MOISTURE. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING AND CUSTOMER REPORTS DISPLAY WAS BLANK CURRENTLY. CUSTOMER STATED THE DISPLAY WAS NOT BLANK LESS THAN 30 SECONDS AND DID NOT RETURNED. THE CUSTOMER REMOVES THE BATTERY AND STATED THE INSERT BATTERY ALARM DID NOT DISPLAY ON THE INSULIN PUMP SCREEN. CUSTOMER STATED THE CONTACT ON THE BATTERY CAP WAS NEITHER MISSING NOR DAMAGE. CUSTOMER STATED BATTERY COMPARTMENT WAS NEITHER DAMAGED NOR CORRODED. CUSTOMER STATED THE SPRING WAS NEITHER DAMAGED NOR CORRODED. CUSTOMER STATED THAT DISPLAY DID NOT RETURNED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10372499 ↗
• InjuryAug 4, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE LEVEL. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 427 MG/DL. CUSTOMER REPORTED THAT THE INSULIN PUMP HAD NO DELIVERY ALARM. CUSTOMER REPORTED THAT THE INSULIN WAS EXITED DURING 5 UNIT FIXED PRIME. CUSTOMER DID NOT ALLEGE UNDER DELIVERING. CUSTOMER DECLINED TO TROUBLESHOOT. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 10360686 ↗
• MalfunctionJul 17, 2020Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD BUTTON ERROR ALARM. CUSTOMER STATED THAT BUTTONS WERE NOT RESPONDING. 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 10287906 ↗
• MalfunctionJul 14, 2020Failure to Cycle; Failure to Cycle

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP ALARMED COMPROMISED FORCE SENSOR SYSTEM. THE CUSTOMER STATED THAT THE ALARM OCCURRED DURING MANUAL PRIME. CUSTOMER REPORTED DRIVE SUPPORT CAP WAS 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 10270460 ↗
• MalfunctionJul 6, 2020Premature Discharge of Battery; Device Difficult to Program or Calibrate; Premature Discharge of Battery; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD BUTTON ERROR AND KEYPAD ISSUE. 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 10231372 ↗
• MalfunctionMay 14, 2020No Display/Image; No Display/Image

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD NO POWER AFTER INSERTING ANOTHER NEW BATTERY. THE CUSTOMER ALSO REPORTED THAT NONE OF THE BUTTONS WERE RESPONDING. THE CUSTOMER ALSO REPORTED THAT THE TIME WAS NOT ADVANCES. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10055241 ↗
• MalfunctionMay 5, 2020Display or Visual Feedback Problem; Device Difficult to Program or Calibrate; Display or Visual Feedback Problem; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE UP ARROW BUTTON OF INSULIN PUMP WAS NOT WORKING, HAD TO USE DOWN BUTTON ONLY. THE CUSTOMER STATED THAT SCREEN OF INSULIN PUMP WAS FOGGY AND UNCLEAR BUT HAD NOT CAUSED ANY ISSUES. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. TROUBLESHOOTING WAS DECLINED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10026345 ↗
• InjuryFeb 18, 2020Premature Discharge of Battery; Device Difficult to Program or Calibrate; No Apparent Adverse Event; Premature Discharge of Battery; Device Difficult to Program or Calibrate; No Apparent Adverse Event

  CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED LOW BLOOD GLUCOSE LEVEL AND INSULIN PUMP RECEIVED UNEXPECTED RESTART, A COLD RESET WAS PERFORMED ALARM AND A BUTTON ERROR ALARM. CUSTOMER'S BLOOD GLUCOSE VALUE WAS 44 MG/DL. CUSTOMER STATED SHE WAS JUST LOW AND WANTS TO DECLINE TROUBLESHOOTING. CUSTOMER STATED THAT THEY OBSERVED TIME CLOCK FOR ONE MINUTE TIME ADVANCED. CUSTOMER STATED THEY ARE NOT ABLE TO CLEAR THE ERROR. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hypoglycemia

  MAUDE report 9719748 ↗
• MalfunctionFeb 10, 2020Computer Software Problem; Device Difficult to Program or Calibrate; Computer Software Problem; Device Difficult to Program or Calibrate

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP¿S ACT BUTTON DID NOT WORKING AND DID NOT ALLOWING CUSTOMER TO DELIVER BOLUS. CUSTOMER STATED THAT THE TIME WAS 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 9686118 ↗
• MalfunctionFeb 6, 2020Display or Visual Feedback Problem; Battery Problem; Connection Problem; Patient Device Interaction Problem; Display or Visual Feedback Problem; Battery Problem; Connection Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD BROKEN PLASTIC NEAR RESERVOIR MAKING IT DIFFICULT TO PLACE INTO THE PUMP. CUSTOMER ALSO REPORTED DIMINISHED BATTERY LIFE. 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 9674914 ↗
• MalfunctionJan 23, 2020Display or Visual Feedback Problem; Power Problem; Insufficient Device Problem Information; Priming Problem; Display or Visual Feedback Problem; Power Problem; Insufficient Device Problem Information; Priming Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN WAS SQUIRTING OUT WHEN PRIMING. CUSTOMER STATED THAT THE INSULIN PUMP REJECTED NEW BATTERIES. CUSTOMER STATED THAT THE INSULIN PUMP HAD NO DELIVERY ALARM. CUSTOMER STATED THAT THE INSULIN PUMP SCREEN HAD BLOTCHES AND RAINBOW EFFECT. NO HARM REQUIRING MEDICAL INTERVENTION REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR THE ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9621175 ↗
• MalfunctionJan 14, 2020Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THE INSULIN PUMP ALARMED MOTOR ERROR. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER STATED THAT THE INSULIN PUMP OFTEN REJECTS NEW CARTRIDGES AND HAD TO REWIND MORE THAN ONCE. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9588829 ↗
• InjuryDec 20, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  CUSTOMER REPORTED VIA PHONE CALL OF EXPERIENCING LOW BLOOD GLUCOSE OF 19 MG/DL AND TREATED WITH GLUCAGON. CUSTOMER WAS TAKEN TO THE HOSPITAL VIA EMERGENCY MEDICAL RESPONSE. CUSTOMER WAS TAKEN TO THE HOSPITAL ON (B)(6) 2019 WITH BLOOD GLUCOSE OF 19 MG/DL; CUSTOMER WAS NOT HOSPITALIZED. CUSTOMER REMOVED THE INSULIN PUMP AND STOPPED USING IT. TROUBLESHOOTING WAS PERFORMED. INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hypoglycemia

  MAUDE report 9501506 ↗
• MalfunctionDec 13, 2019No Display/Image; No Display/Image

  CUSTOMER¿S MOTHER REPORTED VIA PHONE CALL THAT THE CUSTOMER CHANGED THE BATTERY AND THEN THE INSULIN PUMP DID NOT POWER ON ANYMORE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. CUSTOMER DID NOT CALLED BACK AFTER RECEIVING A NEW BATTERY CAP. CUSTOMER STATED THAT THE DISPLAY WAS BLANK CURRENTLY. CUSTOMER STATED THAT THE CONTACT ON THE BATTERY CAP WAS NEITHER MISSING NOR DAMAGE. CUSTOMER STATED THAT THE BATTERY COMPARTMENT WAS NEITHER DAMAGED NOR CORRODED. CUSTOMER STATED THAT THE SPRING WAS NEITHER DAMAGED NOR CORRODED. CUSTOMER STATED THAT THE DISPLAY DID NOT RETURN AFTER INSULIN PUMP RESTART. CUSTOMER STATED THAT THE INSULIN PUMP HAD NOT BEEN DROPPED OR BUMPED RECENTLY. CUSTOMER STATED THAT THE INSULIN PUMP HAD NOT BEEN EXPOSED TO MOISTURE RECENTLY. 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 9465175 ↗
• MalfunctionDec 4, 2019Device Difficult to Program or Calibrate; Obstruction of Flow; Device Difficult to Program or Calibrate; Obstruction of Flow

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP BUTTONS HARD TO PRESS AND NO DELIVERY ALARM. 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 9407846 ↗
• MalfunctionDec 4, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT INSULIN PUMP ALARMED MOTOR ERROR. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER REPORTED THAT THE DRIVE SUPPORT CAP APPEARED NORMAL. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. THE CUSTOMER WAS ADVISED THAT THE PUMP WILL NEED TO BE REPLACED AND WAS ADVISED TO DISCONTINUE USE OF THE 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 9407840 ↗
• MalfunctionNov 26, 2019Excess Flow or Over-Infusion; Power Problem; Patient Device Interaction Problem; Excess Flow or Over-Infusion; Power Problem; Patient Device Interaction Problem

  THE CUSTOMER CALLED AND REPORTED THAT THEIR INSULIN PUMP WAS DELIVERING MORE INSULIN THAN NECESSARY. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER REPORTED THE PUMP WAS REJECTING NEW BATTERIES, HAD A SCRATCHED DISPLAY. TROUBLESHOOTING WAS NOT COMPLETED AS THE CUSTOMER DECLINED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9375191 ↗
• MalfunctionNov 12, 2019Mechanical Problem; Power Problem; Patient Device Interaction Problem; Mechanical Problem; Power Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF INCIDENT. CUSTOMER STATED THAT THE INSULIN PUMP HAD TO REWIND MULTIPLE TIMES. CUSTOMER STATED THAT INSULIN PUMP SCREEN HAD SCRATCHES DEEP, CLEAR ACROSS SCREEN AROUND TO RESERVOIR. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9309218 ↗
• MalfunctionNov 12, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Mechanical Problem; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD KEYPAD ANOMALY AND MOTOR ERROR. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 308 MG/DL. THE CUSTOMER REPORTED THAT THEY HAD RECEIVED MOTOR ERROR FOUR TIMES AND THE ACT BUTTON DOES NOT WANT TO WORK HALF THE TIME. THE CUSTOMER REPORTED THAT THE TIME CLOCK WAS ADVANCING. 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 9309045 ↗
• MalfunctionNov 12, 2019Patient Device Interaction Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY HAD ISSUES WITH SCREWING THE RESERVOIR INTO THE RESERVOIR COMPARTMENT AND SHE HAD TO TRY MULTIPLE TIMES BEFORE THE RESERVOIR GOES IN. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN. INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9307922 ↗
• MalfunctionOct 20, 2019Failure to Cycle; Failure to Cycle

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP ALARMED COMPROMISED FORCE SENSOR SYSTEM. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 101 MG/DL. 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 NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9212397 ↗
• MalfunctionOct 5, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT BUTTONS HAD TO PRESS MORE THAN ONCE AND HARDER TO GET INSULIN PUMP TO RESPOND. THE CUSTOMER'S BLOOD GLUCOSE VALUE 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 9159845 ↗
• MalfunctionOct 1, 2019Mechanical Problem; Patient Device Interaction Problem; Mechanical Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THERE WAS CRACK AROUND THE RESERVOIR COMPARTMENT AND MULTIPLE PIECES CHIPPED. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER DECLINED TO REPORT TO MEDTRONIC 24 HOUR TECHNICAL SUPPORT DEPARTMENT. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9138441 ↗
• MalfunctionSep 18, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Power Problem; Patient Device Interaction Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Battery Problem; Power Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP BUTTONS WERE HARD TO PUSH, STICKY OR SOMETIMES UNRESPONSIVE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER STATED THAT INSULIN PUMP BATTERY LIFE WAS DIMINISHED AND REJECTED NEW BATTERIES. INSULIN PUMP HAD SCRATCHES OR RAINBOW EFFECT ON THE SCREEN. INSULIN PUMP HAD RANDOM NO DELIVERY ALARM AND CRACK TO THE RESERVOIR TOP PART. CUSTOMER WAS DECLINED TROUBLESHOOTING. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9081410 ↗

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