Paradigm® REAL-Time Revel™ MMT-723NAH (UDI 00613994743909)Recalls & reported problems

Summary

The FDA's MAUDE database contains 42 adverse event reports that list this exact device (DI 00613994743909), received between Jun 29, 2017 and Jul 10, 2020 — classified as 13 injuries, 29 malfunctions.

The most frequently reported specific device problem is “Device Displays Incorrect Message” (14 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 42 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 10, 2020Insufficient Flow or Under Infusion; Insufficient Flow or Under Infusion

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP SOMETIMES DID NOT DELIVER INSULIN. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP AND RESERVOIR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10256184 ↗
• InjuryMay 27, 2020Mechanical Problem; Detachment of Device or Device Component; No Apparent Adverse Event; Patient Device Interaction Problem; Mechanical Problem; Detachment of Device or Device Component; No Apparent Adverse Event; Patient Device Interaction Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT THEY WERE HOSPITALIZED ON MAY 18 DUE TO HYPERGLYCEMIA AND DIABETIC KETOACIDOSIS. CUSTOMERS BLOOD GLUCOSE LEVEL WAS 580 MG/DL AT THE TIME OF HOSPITALIZATION. CUSTOMER HAS BEEN USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE LEVEL. CUSTOMER DECLINED TROUBLESHOOTING. CUSTOMER EXPERIENCED SYMPTOMS SUCH AS SHORT OF BREATH AND VOMITING. CUSTOMER WAS TREATED WITH INTRAVENOUS FLUID AND INSULIN DRIP. CUSTOMER DECLINED TO PERFORM A CARELINK UPLOAD. CUSTOMER STATED THAT DRIVE SUPPORT WAS FLUSH. CUSTOMER REPORTED THAT INSULIN PUMP HAD MOTOR ERROR AND TRIED REWINDING BUT DID NOT WORK. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS WHILE THE RESERVOIR WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Dyspnea; Elevated Ketones/ Diabetic Ketoacidosis; Hyperglycemia; Vomiting

  MAUDE report 10091095 ↗
• MalfunctionMay 5, 2020Use of Device Problem; Power Problem; Patient Device Interaction Problem; Priming Problem; Use of Device Problem; Power Problem; Patient Device Interaction Problem; Priming Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD DIMINISHED BATTERY LIFE, LOST INSULIN PUMP SETTING, DATE AND TIME DURING BATTERY WAS CHANGE, CRACK ON TOP CORNER OF INSULIN PUMP SCREEN, MULTIPLE PRIMING NEEDED TO GET TUBING TO FILL. 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 10023025 ↗
• MalfunctionApr 29, 2020Failure to Cycle; Detachment of Device or Device Component; Failure to Cycle; Detachment of Device or Device Component

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A COMPROMISED FORCE SENSOR SYSTEM ALARM AND 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 10008424 ↗
• MalfunctionFeb 25, 2020Failure to Cycle; Detachment of Device or Device Component; Failure to Cycle; Detachment of Device or Device Component

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD COMPROMISED FORCE SENSOR SYSTEM ERROR DURING PRIMING. CUSTOMER STATED THAT THE INSULIN WAS SQUIRTING OUT. CUSTOMER REPORTED THAT THE DRIVE SUPPORT CAP WAS STICKING OUT. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9749608 ↗
• MalfunctionDec 26, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR ALARMS AND REWIND WAS LOUDER AND SLOWER. 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 9518176 ↗
• InjuryDec 18, 2019Mechanical Problem; Mechanical Problem

  CUSTOMER'S HUSBAND REPORTED VIA PHONE CALL THAT INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER ALSO REPORTED THAT HIS WIFE EXPERIENCED HIGH BLOOD GLUCOSE LEVEL OF 485 MG/DL. CUSTOMER HAD NOT BEEN USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE EVENT. THE CUSTOMER ASKED ABOUT ASSISTANCE ON HOW TO ADMINISTER BOLUS. THE INSULIN PUMP WAS RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9485997 ↗
• MalfunctionDec 16, 2019Mechanical Problem; Obstruction of Flow; Mechanical Problem; Obstruction of Flow

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER DECLINED TROUBLESHOOTING FOR MOTOR ERROR. INSULIN PUMP HAD TO CONSTANTLY REWIND OR RE PRIME MULTIPLE TIMES, HAD NO DELIVERY ALARM. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9471961 ↗
• InjuryNov 25, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  CUSTOMER¿S HUSBAND REPORTED VIA PHONE CALL THAT THE CUSTOMER EXPERIENCED A HIGH BLOOD GLUCOSE. CUSTOMER¿S HIGH BLOOD GLUCOSE VALUE WAS OVER 600 MG/DL. CUSTOMER WAS ADVISE TO MONITOR THE BLOOD GLUCOSE AND IF AFTER 30 TO 45 MINUTES IF IT¿S STILL OVER 600 MG/DL THEN CALL HEALTH CARE PROFESSIONAL FOR SUGGESTION HOW MUCH MANUAL INJECTION TO TAKE. CUSTOMER DECLINE TROUBLESHOOTING FOR HIGH BLOOD GLUCOSE. THE DEVICE WILL NOT RETURN FOR THE ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9368152 ↗
• MalfunctionSep 18, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE FOLLOWING DEVICE WERE OR MAY BE THE SUBJECT OF LITIGATION. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER REPORTED THAT THE DEVICE UNDER THIS LEGAL HOLD MAY NOT BE DESTRUCTIVELY ANALYZED WITHOUT WRITTEN APPROVAL FROM THE CORPORATE LITIGATION DEPARTMENT. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9080133 ↗
• MalfunctionAug 13, 2019Detachment of Device or Device Component; Patient Device Interaction Problem; Detachment of Device or Device Component; Patient Device Interaction Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT THE DRIVE SUPPORT CAP POPS OUT DURING REWIND AND BUTTONS COVER WAS BROKEN. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN. CUSTOMER STATED INSULIN PUMP WAS DAMAGE AND HELD TOGETHER BY TAPE. CUSTOMER STATED THAT NO PHYSICAL DAMAGED TO THE RESERVOIR LIP RING. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8887182 ↗
• InjuryJun 14, 2019Device Difficult to Program or Calibrate; No Apparent Adverse Event; Device Difficult to Program or Calibrate; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HYPERGLYCEMIA AND THE ACT BUTTON WAS NOT RESPONDING. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 555 MG/DL AT THE TIME OF THE INCIDENT AND WAS TREATED WITH MANUAL INJECTIONS. THE CUSTOMER DECLINED TROUBLESHOOTING FOR HIGH GLUCOSE. IT WAS REPORTED THAT THE CUSTOMER REWOUND THE INSULIN PUMP, BUT AFTER THE INSULIN PUMP REWOUND THE INSULIN PUMP WAS NOT RESPONDING TO THE ACT BUTTON TO PRIME. 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: Hyperglycemia

  MAUDE report 8698938 ↗
• InjuryJun 4, 2019Failure to Cycle; No Apparent Adverse Event; Failure to Cycle; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED THE HIGH BLOOD GLUCOSE. THE CUSTOMER BLOOD GLUCOSE LEVEL WAS 400 MG/DL AT THE TIME OF INCIDENT. THE CUSTOMER STATED THAT THE INSULIN PUMP HAD COMPROMISED FORCE SENSOR SYSTEM ALARM. THE CUSTOMER STATES THAT THE DRIVE SUPPORT CAP APPEARS NORMAL. THE CUSTOMER DECLINED THE TROUBLESHOOTING FOR HIGH BLOOD GLUCOSE. THE CUSTOMER DID NOT PROVIDE ANY INFORMATION REGARDING SYMPTOMS AND TREATMENT FOR THEIR HIGH BLOOD GLUCOSE. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND TO REVERT TO THE BACK-UP PLAN. THE CUSTOMER WAS ADVISED THE PUMP WILL BE REPLACED AS PER TROUBLESHOOT. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 8665287 ↗
• MalfunctionMay 1, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER'S MOTHER REPORTED VIA PHONE THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF INCIDENT. CUSTOMER WAS ABLE TO SUCCESSFULLY CLEAR THE ALARM ALSO ABLE TO COMPLETE PUMP REWIND. CUSTOMER STATED THE DRIVE SUPPORT CAP APPEARS NORMAL. CUSTOMER STATED IN THE ALARM HISTORY INSULIN PUMP HAD MOTOR POSITION ENCODER ERROR ALARM ALSO MORE THAN ONE MOTOR ERROR ALARM WITHIN A 30-DAY PERIOD. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8567719 ↗
• MalfunctionFeb 18, 2019Connection Problem; Patient Device Interaction Problem; Connection Problem; Patient Device Interaction Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT THE RESERVOIR WAS NOT ABLE TO LOCK IN PLACE WHEN INSERTED INTO INSULIN PUMP. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 164 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. 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 8346931 ↗
• MalfunctionFeb 5, 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 155 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER STATED THAT THE DRIVE SUPPORT CAP WAS APPEARS 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. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8307242 ↗
• MalfunctionNov 8, 2018Failure to Cycle; Failure to Cycle

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD RECEIVED NOT STOP SQUIRTING INSULIN OUT OF THE TUBING DURING PRIMING. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. CUSTOMER STATED THAT THE INSULIN PUMP HAD TO TAKE OUT THE BATTERY OF THE INSULIN PUMP TO GET IT TO STOP AND SHE WAS TRIED TO START THE INSULIN PUMP AGAIN THREE TIMES BUT SAME THING HAPPENED AGAIN. CUSTOMER ALSO STATED THAT THE INSULIN PUMP WAS OFF. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8050120 ↗
• MalfunctionSep 21, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE DRIVE SUPPORT CAP WAS DAMAGED. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 244 MG/DL AT THE TIME OF INCIDENT. CUSTOMER STATES THAT MOTOR HAD BEEN POPPING OUT OF THE PUMP TROUBLESHOOTING WAS PERFORMED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7897441 ↗
• MalfunctionAug 27, 2018Failure 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 UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER ALSO REPORTED THAT THE INSULIN WAS SQUIRTING DURING MANUAL PRIME PROCESS. THE CUSTOMER STATED THAT THE DRIVE SUPPORT CAP WAS 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. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7815802 ↗
• MalfunctionJul 19, 2018Obstruction of Flow; Obstruction of Flow

  THE CUSTOMER REPORTED VIA PHONE CALL THAT INSULIN PUMP HAD NO DELIVERY ALARM. THE BLOOD GLUCOSE AT THE TIME OF THE INCIDENT WAS 376 MG/DL. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 7705266 ↗
• MalfunctionJun 22, 2018Crack; Application Interface Becomes Non-Functional Or Program Exits Abnormally; Fluid/Blood Leak; Device Displays Incorrect Message; Battery Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD SEVERAL ISSUES. CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF INCIDENT. CUSTOMER REPORTED CRACKS AND CHIPPING IN THE INSULIN PUMP CASING AND RESERVOIR COMPARTMENT, INSULIN SQUIRTS OUT, DURING PRIMING, HAD A FAILED BATTERY TEST ALARM AND THE BUTTONS WERE LESS RESPONSIVE. NO TROUBLESHOOTING WAS PERFORMED. INSULIN PUMP IS NOT EXPECTED TO RETURN FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7628908 ↗
• InjuryJun 5, 2018Fluid/Blood Leak; Device Displays Incorrect Message; Material Protrusion/Extrusion

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP ALARMED COMPROMISED FORCE SENSOR SYSTEM. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 334 MG/DL. THE CUSTOMER ALSO REPORTED THAT THE INSULIN WAS SQUIRTING DURING MANUAL PRIME PROCESS. TROUBLESHOOTING WAS PERFORMED FOR PRIME REWIND. THE DRIVE SUPPORT CAP WAS PROTRUDED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 7568320 ↗
• MalfunctionFeb 6, 2018Sticking

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP ALARMED COMPROMISED FORCE SENSOR SYSTEM. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 194 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER STATED THAT THE DRIVE SUPPORT CAP WAS STICKING OUT. 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 7246484 ↗
• MalfunctionFeb 6, 2018Device Displays Incorrect Message

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP WAS DIED WITHOUT WARNING. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER WAS NOT ABLE TO DO ANY TROUBLESHOOTING. INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7245043 ↗
• InjuryFeb 2, 2018Device Displays Incorrect Message

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY GOT ERROR ALARMS ON INSULIN PUMP. THE CUSTOMER'S BLOOD GLUCOSE WAS 468 MG/DL. CUSTOMER STATED THE ALARM DID NOT OCCUR RIGHT AFTER A 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: Hyperglycemia

  MAUDE report 7235348 ↗

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-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-1587-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-522
• Z-1593-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723K
• Z-1594-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723
• Z-1590-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-722K
• Z-1591-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-523
• 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