Paradigm® REAL-Time Revel™ MMT-723NAB (UDI 00643169446434)Recalls & reported problems

Summary

The FDA's MAUDE database contains 322 adverse event reports that list this exact device (DI 00643169446434), received between Jun 3, 2017 and Aug 25, 2020 — classified as 2 deaths, 111 injuries, 209 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (49 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 322 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 25, 2020Obstruction of Flow; Battery Problem; Patient Device Interaction Problem; Obstruction of Flow; Battery Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE BATTERY LIFE OF THE INSULIN PUMP WAS SHORTER AND HAD TO CHANGE IT IN EVERY 3 TO 4 WEEKS. CUSTOMER HAD EXPERIENCED BATTERY DRAINING AND INSULIN PUMP DYING WHEN HE FIRST GOT WARNING OF LOW BATTERY. THERE WAS A CRACK IN TOP RIGHT CORNER OUTSIDE OF SCREEN BY BUTTON. THERE WERE ALSO NO DELIVERY ALARMS ON THE SCREEN. 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 10446740 ↗
• MalfunctionJun 17, 2020Mechanical Problem; Obstruction of Flow; Patient Device Interaction Problem; Mechanical Problem; Obstruction of Flow; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER STATED THAT THE INSULIN PUMP HAD NO DELIVERY ALARMS. CUSTOMER STATED THAT THE SCREEN WAS SCRATCHED. INSULIN PUMP WAS SLOWER TO 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 10161490 ↗
• MalfunctionJun 8, 2020Mechanical Problem; Obstruction of Flow; Detachment of Device or Device Component; Patient Device Interaction Problem; Mechanical Problem; Obstruction of Flow; Detachment of Device or Device Component; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP RECEIVED MOTOR ERROR ALARM. THE BATTERY LIFE WAS DIMINISHED AND INSULIN PUMP ALSO RECEIVED NO DELIVERY ALARM AND RESERVOIR CASING WAS DAMAGED. CUSTOMER STATED DRIVE SUPPORT CAP WAS DAMAGED. THE CUSTOMER STATED THAT EXTERIOR PART OF CASE POPPED OUT, WHERE THE RESERVOIR GOES IN AND PIECE OF INSULIN PUMP WAS LOOSE. 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 10126865 ↗
• MalfunctionMay 13, 2020Mechanical Problem; Mechanical Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER WAS ABLE TO REWIND THE INSULIN PUMP AND 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 10054585 ↗
• MalfunctionApr 28, 2020Obstruction of Flow; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP RECEIVED NO DELIVERY ALARM. CUSTOMER STATED THAT THE TUBING WAS NOT BENT OR KINKED. CUSTOMER STATED THAT THEY TRIED ALL REMEDIES. 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 10003775 ↗
• MalfunctionApr 23, 2020No Display/Image; No Display/Image

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP DISPLAY WAS BLANK. CUSTOMER BLOOD GLUCOSE READING WAS 222 MG/DL. TROUBLESHOOTING WAS PERFORMED. CUSTOMER DID NOT MENTIONED THE CAUSE OF THE BLANK DISPLAY. THE CUSTOMER INSERTED NEW BATTERY BUT THE ISSUE REOCCURRED. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9991490 ↗
• MalfunctionApr 7, 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 THEY WERE UNABLE TO EXIT THE PREPARING TO PRIME LOOP. THE DEVICE WAS NOT BUMPED OR DROPPED PRIOR TO THE ALARM AND 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 9932376 ↗
• MalfunctionApr 6, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER STATED 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 Known Impact Or Consequence To Patient

  MAUDE report 9931540 ↗
• MalfunctionMar 19, 2020Patient Device Interaction Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT CRACKED ON THE FRONT OF THE INSULIN. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9851740 ↗
• InjuryMar 18, 2020Adverse Event Without Identified Device or Use Problem; Appropriate Device Problem Term/Code Not Available; Adverse Event Without Identified Device or Use Problem; Appropriate Device Problem Term/Code Not Available

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 411 MG/DL. THE CUSTOMER DECLINED TROUBLESHOOTING FOR HIGH BLOOD GLUCOSE. CUSTOMER HAS BEEN USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE EVENT. CUSTOMER STATED THAT INSULIN PUMP HAD LOW BATTERY ALARM. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9847267 ↗
• MalfunctionMar 4, 2020Battery Problem; Battery Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD ERROR ALARM. BATTERIES DYING QUICKER. 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 9784792 ↗
• MalfunctionFeb 18, 2020Device Difficult to Program or Calibrate; Power Problem; Patient Device Interaction Problem; Device Difficult to Program or Calibrate; Power Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE SCRATCHES ON INSULIN PUMP SCREEN MAKING IT HARDER TO READ. SEVERAL TIMES RECEIVED RANDOM OR UNEXPLAINED NO DELIVERY ALARMS. CUSTOMER REPORTED THAT THE INSULIN PUMP HAD REJECTED BATTERIES, BUTTONS PRESS MORE THAN ONCE TO GET INSULIN PUMP TO RESPOND. 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 9724320 ↗
• MalfunctionJan 24, 2020Mechanical Problem; Obstruction of Flow; Battery Problem; Mechanical Problem; Obstruction of Flow; Battery Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR AND UNEXPLAINED NO DELIVERY. 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 9625815 ↗
• MalfunctionDec 24, 2019Device Difficult to Program or Calibrate; Device Difficult to Program or Calibrate

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE BUTTONS ON INSULIN PUMP WAS HARD TO PUSH. 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: Hyperglycemia

  MAUDE report 9515940 ↗
• MalfunctionDec 23, 2019Mechanical Problem; Patient Device Interaction Problem; Mechanical Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD DAMAGE AND ALARMED MOTOR ERROR. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS NOT REPORTED. THE DEVICE WAS RETURNED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9509651 ↗
• MalfunctionDec 4, 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 HAD MOTOR ERROR, UNEXPLAINED NO DELIVERY ALARM AND BUTTONS HAD TO PRESS TO TWICE. 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 9409347 ↗
• MalfunctionNov 26, 2019Failure 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; THE INSULIN SQUIRTED OUT DURING THE MANUAL PRIME PROCESS AND THE DRIVE SUPPORT CAP WAS STICKING OUT. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER STATED THAT THE INSULIN CONTINUED TO DRIP AFTER MOTOR STOPS DURING THE MANUAL PRIME PROCESS. THE CUSTOMER WAS UNABLE TO EXIT THE PREPARING TO PRIME LOOP. THE CUSTOMER STATED THAT THE REWIND MESSAGE OCCURRED AFTER AN ALARM OR ALERT. THE CUSTOMER STATED THAT THEY WERE STUCK IN REWIND COMPLETE/BOLUS DELIVERY LOOP. 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 9374890 ↗
• MalfunctionNov 19, 2019Obstruction of Flow; Power Problem; Patient Device Interaction Problem; Obstruction of Flow; Power Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP SHUTS OFF ON ITS OWN, AND HAS TO RESET IT. THE CUSTOMER'S BLOOD GLUCOSE WAS UNKNOWN. THE CUSTOMER REPORTED CRACKS ON THE TOP AND THE BOTTOM AND INSULIN PUMP RECEIVED NO DELIVERY ALERT. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9340532 ↗
• InjuryNov 18, 2019Obstruction of Flow; Obstruction of Flow

  THE CUSTOMER¿S MOTHER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE LEVEL. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS ABOVE 600 MG/DL. THE CUSTOMER DID NOT MENTION ANY SYMPTOM RELATED TO HIGH BLOOD GLUCOSE LEVEL. THE CUSTOMER STATED THAT THEY TREATED HIGH BLOOD GLUCOSE LEVEL WITH MANUAL INJECTIONS. THE CUSTOMER MENTIONED THAT THE INSULIN PUMP HAD NO DELIVERY ALARM WHICH WAS RESOLVED BY INFUSION SET CHANGE. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9333754 ↗
• MalfunctionNov 17, 2019No Display/Image; Power Problem; No Display/Image; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP DIED. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 176 MG/DL. THE INSULIN PUMP WAS NOT BUMPED, DROPPED OR EXPOSED TO MOISTURE. CUSTOMER STATED THE CONTACTS ON THE BATTERY CAP WERE NOT MISSING OR DAMAGED. CUSTOMER STATED BATTERY COMPARTMENT WAS NEITHER DAMAGED NOR CORRODED. CUSTOMER STATED THAT THE SPRING WAS NEITHER DAMAGED NOR CORRODED. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING AND DISPLAY RETURNED BACK. THE INSULIN PUMP¿S DISPLAY RETURNED WITH A FAILED BATTERY TEST ALERT THEN SHUT BACK OFF. ADVISED CUSTOMER IF NOT ALIGNED OR TIGHTENED THE INSULIN PUMP MAY ALARM FAILED BATTERY TEST. CUSTOMER DID NOT RECEIVE FAILED BATTERY TEST. CUSTOMER RECEIVED A WEAK BATTERY ALERT THEN THE INSULIN PUMP SHUT BACK OFF. CUSTOMER WAS ABLE TO SUCCESSFULLY CLEAR THE ALARM. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9333713 ↗
• MalfunctionNov 11, 2019Device Difficult to Program or Calibrate; Material Integrity Problem; Adverse Event Without Identified Device or Use Problem; Device Difficult to Program or Calibrate; Material Integrity Problem; 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 UNKNOWN. THE CUSTOMER REPORTED THAT THE BUTTONS WERE HARD TO PRESS AND ALSO HAD NO DELIVERY ALARM. THE CUSTOMER REPORTED THAT HE EVENT WAS RESOLVED BY CHANGING COMPLETE SET (INFUSION SET AND RESERVOIR). 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 9304463 ↗
• MalfunctionNov 11, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Mechanical Problem; Device Difficult to Program or Calibrate

  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 WAS ABLE TO REWIND. CUSTOMER STATED THAT THE INSULIN PUMP HAD BUTTON ERROR ALARM. DRIVE SUPPORT CAP WAS NORMAL. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9304415 ↗
• DeathNov 4, 2019Adverse 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 AT HOME. THE CAUSE OF DEATH WAS A HEART ATTACK. THE CALLER STATED THAT THE CUSTOMER HAD NO OTHER ILLNESSES THAT MAY HAVE LED TO THE CUSTOMER'S PASSING. THE CUSTOMER¿S BLOOD GLUCOSE WAS LOW ENOUGH NOT TO REGISTER ON A METER AT THE TIME OF DEATH. THE CUSTOMER WAS NOT WEARING THE INSULIN PUMP AT THE TIME OF DEATH DUE TO A LOW. THE INSULIN PUMP HAD BEEN DISCONNECTED SHORTLY BEFORE PASSING. THE CUSTOMER WAS NOT USING MEDTRONIC SENSORS. THE CUSTOMER WAS USING A COMPETITOR'S SENSOR SYSTEM. THE CUSTOMER'S BROTHER HEARD THE CUSTOMER'S PUMP GOING OFF AND THE CUSTOMER WAS HAVING A LOW. THE CUSTOMER WAS GIVEN JUICE AND GLUCOSE TABLETS BUT THEY HAD TO CALL PARAMEDICS. THE CALLER DECLINED TO RETURN THE INSULIN PUMP FOR ANALYSIS.

  Patient problems: Death; Hypoglycemia

  MAUDE report 9276416 ↗
• MalfunctionOct 23, 2019Mechanical Problem; Obstruction of Flow; Battery Problem; Power Problem; Appropriate Device Problem Term/Code Not Available; Patient Device Interaction Problem; Priming Problem; Mechanical Problem; Obstruction of Flow; Battery Problem; Power Problem; Appropriate Device Problem Term/Code Not Available; Patient Device Interaction Problem; Priming Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP'S BELT CLIP WAS BROKEN, THERE WERE SCRATCHES ON THE INSULIN PUMP, BATTERY LIFE WAS DIMINISHED AT 3 WEEKS, INSULIN PUMP HAD REJECTED NEW BATTERIES, HAD NO DELIVERY ALARMS NECESSITATING SITE CHANGE, INSULIN PUMP REWINDING SEEMED TO BE TAKING LONGER AND INSULIN PUMP SQUIRTED OUT INSULIN DURING PRIMING INSTEAD OF DRIPPING. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9227513 ↗
• MalfunctionOct 16, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 191 MG/DL. THE DRIVE SUPPORT CAP WAS NORMAL. CUSTOMER REPORTED THAT THEY USING PHONE THAT HAD MAGNETIC CLASP WHILE INQUIRED ABOUT INSULIN PUMP EXPOSURE TO MAGNETIC FIELD. CUSTOMER WAS ABLE TO REWIND THE INSULIN PUMP. CUSTOMER WAS ABLE TO CLEAR THE ALARM. THE CUSTOMER WAS ADVISED TO DISCONTINUED 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 9197163 ↗

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-1591-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523
• Z-1587-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-522
• Z-1589-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-522K
• Z-1590-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-722K
• 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-1588-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-722
• 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