Paradigm® REAL-Time Revel™ MMT-723LNAS (UDI 00643169478602)Recalls & reported problems

Summary

The FDA's MAUDE database contains 156 adverse event reports that list this exact device (DI 00643169478602), received between Jun 8, 2017 and Jul 30, 2020 — classified as 3 deaths, 46 injuries, 107 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (32 reports).

1 FDA recall record name this device's identifier, 1 still open.

13 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.

Recalls naming this device

1. Feb 13, 2026Class IIOpen, Classified

   All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

   Z-1750-2026 · Root cause: Device Design · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 25 most recent of 156 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 30, 2020No Display/Image; No Display/Image

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD BLANK DISPLAY. CUSTOMER STATED THAT THE DISPLAY WAS BLANK LESS THAN 30 SECONDS AND THEN RETURNED. CUSTOMER STATED THAT ABOUT TWO WEEKS HIS INSULIN PUMP TURNED OFF AND CAME BACK ON AND NOW THE SCREEN WENT BLANK. CUSTOMER STATED THE CONTACTS ON THE BATTERY CAP WERE NEITHER MISSING NOR DAMAGED. DISPLAY DID NOT RETURN AFTER INSERTING NEW BATTERY. 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 10343076 ↗
• MalfunctionJul 20, 2020No Display/Image; Moisture or Humidity Problem; No Display/Image; Moisture or Humidity Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP WAS NOT TURNING ON. CUSTOMER STATED THAT THE INSULIN PUMP WAS EXPOSED TO MOISTURE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

  MAUDE report 10294744 ↗
• MalfunctionJun 24, 2020Mechanical Problem; Mechanical Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER WAS UNABLE TO CLEAR THE ALARM AND UNABLE TO REWIND THE INSULIN PUMP. 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 10187599 ↗
• MalfunctionApr 9, 2020Device Alarm System; Device Alarm System

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP WAS NOT BEEPING. CUSTOMER PERFORMED SELF TEST AND INSULIN PUMP DID NOT BEEP DURING TONE TEST OF THE SELF TEST. 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 9942923 ↗
• MalfunctionApr 9, 2020Failure to Cycle; Mechanical Problem; Priming Problem; Failure to Cycle; Mechanical Problem; Priming Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD COMPROMISED FORCE SENSOR SYSTEM ALARM. IT WAS REPORTED THAT THE PISTON NOT REWINDING AND WAS UNABLE TO COMPLETE THE PRIMING. CUSTOMER STATED THAT THE DRIVE SUPPORT CAP APPEARED 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 9942252 ↗
• MalfunctionApr 8, 2020Mechanical Problem; Mechanical Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP ALARMED MOTOR ERROR. THE INSULIN PUMP WAS BUMPED SEVERAL TIMES. THE DRIVE SUPPORT CAP APPEARED NORMAL. THE CUSTOMER WAS ABLE TO CLEAR AND ABLE TO REWIND 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 9936802 ↗
• MalfunctionFeb 28, 2020Mechanical Problem; Obstruction of Flow; Mechanical Problem; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE PISTON OF THE INSULIN PUMP WAS FROZEN. CUSTOMER STATED THAT THE INSULIN PUMP HAD NO DELIVERY ALARMS. CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING FOR NO DELIVERY ALARMS. CUSTOMER NOT TRIED DIFFERENT CANNULA LENGTHS. CUSTOMER STATED THE TUBING WAS NOT BENT OR KINKED. 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 9768425 ↗
• MalfunctionFeb 24, 2020No Display/Image; Moisture or Humidity Problem; No Display/Image; Moisture or Humidity Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A BLANK DISPLAY IMMEDIATELY AFTER EXPOSED TO WATER. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9744029 ↗
• MalfunctionFeb 3, 2020Failure to Cycle; Failure to Cycle

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A COMPROMISED FORCE SENSOR SYSTEM ALARM AND IT KEPT LOADING. THE CUSTOMER REPORTED THAT THE SCREEN WENT OFF AND IT STARTED COUNTING. THE CUSTOMER WAS ABLE TO CLEAR THE ALARM BUT WAS NOT ABLE TO COMPLETE REWIND. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9658627 ↗
• MalfunctionDec 16, 2019Premature Discharge of Battery; Loss of Data; Premature Discharge of Battery; Loss of Data

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD A MULTIPLE INSULIN PUMP ERROR ALARMS. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 240 MG/DL. THE DRIVE SUPPORT CAP WAS NORMAL. THE CUSTOMER WAS ABLE TO SUCCESSFULLY CLEAR THE ALARM. THE CUSTOMER WAS ABLE TO COMPLETE INSULIN PUMP REWOUND. CUSTOMER STATED THAT THEY RECEIVED ANOTHER UNEXPECTED RESTART ALARM AFTER BATTERY CHANGE. 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 9471970 ↗
• MalfunctionNov 19, 2019Computer Software Problem; Display or Visual Feedback Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Use of Device Problem; Computer Software Problem; Display or Visual Feedback Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Use of Device Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT ACT BUTTON WAS HARDER TO PRESS. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF INCIDENT. CUSTOMER STATED BACKLIGHT WAS DIMMER, MOTOR MADE GRINDING NOISE DURING REWINDING, HAD TO RESET THE ALARMS AND RECEIVED UNEXPLAINED SIREN ALARMS. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9339921 ↗
• MalfunctionOct 18, 2019Power Problem; Power Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP SHUT OFF EVEN AFTER PUTTING IN BRAND NEW BATTERIES. 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 9209025 ↗
• MalfunctionSep 19, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD A MOTOR ERROR ALARM. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER TRIED CLEARING THE MOTOR ALARM, REWINDING IT, AND FILLING CANNULA, BUT WHENEVER THEY FILL CANNULA, IT KEPT ON GETTING MOTOR ERROR. THE CUSTOMER STATED THAT THE DRIVE SUPPORT CAP APPEARED NORMAL OR SLIGHTLY INDENTED. THE CUSTOMER WAS ABLE TO CLEAR THE ALARM SUCCESSFULLY BUT WERE UNABLE TO COMPLETE THE INSULIN PUMP REWIND. 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 9086354 ↗
• MalfunctionSep 13, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Material Integrity Problem; Insufficient Device Problem Information; Patient Device Interaction Problem; Priming Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Material Integrity Problem; Insufficient Device Problem Information; Patient Device Interaction Problem; Priming Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP RECEIVED UNEXPLAINED NO DELIVERY ALERT AND ERROR MESSAGE. THE CUSTOMER BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER ALSO STATED THAT WHEN BUTTONS WERE PUSHED, AND ALSO THOUGHT THAT IT LOUDER WHEN PRIME OR REWIND THAN BEFORE AND ALSO HAD TO PRIME OR REWIND MORE THAN ONCE DUE TO PUSHING THE WRONG THING TO INSULIN PUMP. THE INSULIN PUMP HAD CRACKS ON SCREEN AND THE BATTERY CAP WAS STRIPPING PLASTIC CHIPS OFF AND RESERVOIR TIP WOULD BROKE OFF. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9023702 ↗
• MalfunctionSep 6, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THE INSULIN PUMP ALARMED MOTOR ERROR. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 140 MG/DL AT THE TIME OF THE INCIDENT. CUSTOMER WAS UNABLE TO CLEAR THE ALARM. CUSTOMER WAS UNABLE TO COMPLETE PUMP REWIND. THE CUSTOMER STATED THAT THE DRIVE SUPPORT CAP WAS NORMAL. THE CUSTOMER STATED THAT THE INSULIN PUMP WAS EXPOSED TO X RAY. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND TO REVERT TO THE BACK-UP PLAN. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8968363 ↗
• MalfunctionSep 6, 2019Device Difficult to Program or Calibrate; Patient Device Interaction Problem; Device Difficult to Program or Calibrate; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP'S BUTTONS WERE NOT WORKING. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. CUSTOMER WAS ADVISED TO OBSERVE TIME CLOCK FOR ONE MINUTE TO VERIFY IF TIME ADVANCES AND THEY STATED THAT WORKING AS SUPPOSE TO. 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 8968297 ↗
• MalfunctionSep 5, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Mechanical Problem; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE UP BUTTON WAS NO LONGER WORKING, ACT BUTTON HAD TO BE PRESSED HARD IN ORDER TO RESPOND AND HAD MOTOR ERRORS. 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 8968121 ↗
• MalfunctionAug 28, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE BUTTONS WERE NOT WORKING. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER ALSO REPORTED THAT CLIP WAS BROKEN. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8938956 ↗
• MalfunctionAug 23, 2019Computer Software Problem; Application Program Problem: Dose Calculation Error; Mechanical Problem; Obstruction of Flow; Loss of Data; Computer Software Problem; Application Program Problem: Dose Calculation Error; Mechanical Problem; Obstruction of Flow; Loss of Data

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP ALARMED MULTIPLE ERRORS. THE CUSTOMER'S BLOOD GLUCOSE VALUE WAS 103 MG/DL. THE CUSTOMER ALSO REPORTED THAT THEY RECEIVED MOTOR ERROR AND NO DELIVERY ALERT. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8924763 ↗
• MalfunctionAug 19, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER'S WIFE REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD A MOTOR ERROR ALARM. THE 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 8904914 ↗
• InjuryAug 14, 2019Insufficient Flow or Under Infusion; Appropriate Device Problem Term/Code Not Available; Insufficient Flow or Under Infusion; Appropriate Device Problem Term/Code Not Available

  THE CUSTOMER REPORTED VIA PHONE CALL THAT SHE EXPERIENCED HYPOGLYCEMIA. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS IN THE RANGE OF 40 MG/DL. THE CUSTOMER ALSO REPORTED THAT SHE HAD UNEXPLAINED HIGH BLOOD GLUCOSE LEVEL AND SHE BELIEVED THAT HER INSULIN PUMP WAS NOT ALWAYS DELIVERING THE PROPER BASAL OR BOLUS THAT WAS PROGRAMMED TO DELIVER. THE CUSTOMER'S OTHER BLOOD GLUCOSE LEVEL WAS 300 G/DL. THE CUSTOMER DECLINED TROUBLESHOOTING. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia; Hypoglycemia

  MAUDE report 8892427 ↗
• MalfunctionAug 8, 2019Mechanical Problem; Battery Problem; Communication or Transmission Problem; Mechanical Problem; Battery Problem; Communication or Transmission Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT HIS INSULIN PUMP HAD RECEIVED MOTOR ERROR DAILY OR EVERY OTHER DAY. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER ALSO REPORTED THAT THE BATTERIES DID NOT LAST LONGER THAN 2-3 DAYS AND THE INSULIN PUMP NO LONGER COMMUNICATES WITH THE METER. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8874194 ↗
• MalfunctionJul 31, 2019Premature Discharge of Battery; Moisture or Humidity Problem; Power Problem; Premature Discharge of Battery; Moisture or Humidity Problem; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP WAS NOT WORKING AND HAD UNEXPECTED RESTART ALARM. CUSTOMER¿S BLOOD GLUCOSE WAS 248 MG/DL AT THE TIME OF INCIDENT. CUSTOMER REPORTED THEY WERE UNABLE TO CLEAR THE ALARM. CUSTOMER REPORT INSULIN PUMP DID NOT REQUIRE REWIND. CUSTOMER STATED THERE WAS FLUID UNDER THE SCREEN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8846221 ↗
• MalfunctionJul 25, 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 177 MG/DL AT THE TIME OF THE INCIDENT. CUSTOMER ASSISTED WITH TROUBLESHOOTING AND STATED THAT THEY WERE ABLE TO CLEAR THE ALARM AND ABLE TO COMPLETE INSULIN PUMP REWIND. CUSTOMER PERFORMED DISPLACEMENT TEST AND IT WAS FAILED. THE CUSTOMER WAS ADVISED THAT THE INSULIN PUMP NEEDED TO BE REPLACED AND REVERT TO THE BACKUP PLAN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8825115 ↗
• MalfunctionJun 13, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM MULTIPLE TIMES. CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF INCIDENT. TROUBLESHOOTING WAS NOT PERFORMED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8695055 ↗

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-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-1587-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-522
• Z-1592-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523K
• Z-1589-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-522K
• Z-1594-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723
• 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-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