Paradigm® REAL-Time Revel™ MMT-523NAH (UDI 00643169202313)Recalls & reported problems

Summary

The FDA's MAUDE database contains 36 adverse event reports that list this exact device (DI 00643169202313), received between Jun 6, 2017 and Jul 8, 2021 — classified as 6 injuries, 30 malfunctions.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (6 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 36 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 8, 2021Break; Break

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD A BROKEN RETAINER RING. THE CUSTOMER STATED THAT THE RESERVOIR WAS ABLE TO LOCK INTO PLACE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Insufficient Information

  MAUDE report 12140535 ↗
• MalfunctionAug 6, 2020No Display/Image; Device Difficult to Program or Calibrate; Patient Device Interaction Problem; No Display/Image; Device Difficult to Program or Calibrate; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP WAS KEEP CYCLING THE SELF-TEST AND WAS NOT DISPLAY ALARMS. CUSTOMER ALSO NOTED THE KEYPAD WAS UNRESPONSIVE AND THAT THERE ARE SEVERAL CRACKS IN THE INSULIN PUMP. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. CUSTOMER NOTED CRACKS ARE ALL OVER INSULIN PUMP BUT NOW BATTERY WAS NOT HOLD IN PLACE UNLESS IT WAS HELD IN WITH ELECTRICAL TAPE. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10371729 ↗
• MalfunctionMar 12, 2020No Display/Image; Patient Device Interaction Problem; No Display/Image; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT INSULIN PUMP WAS NO LONGER WORKING AND THERE WAS DAMAGE ON BATTERY CAVITY AND BATTERY DID NOT COME 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 9822359 ↗
• MalfunctionOct 4, 2019Display or Visual Feedback Problem; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem; Display or Visual Feedback Problem; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAS STOP WORKING. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 133 MG/DL. CUSTOMER STATED THAT THE INSULIN PUMP HAD LOW BATTERY AND LOW RESERVOIR. CUSTOMER STATED THAT SHE CHANGED BATTERY AND IT KEEPS GETTING BLACK LINES ACROSS THE DISPLAY SCREEN AND SHE CAN'T SEE ANYTHING TO READ THE DISPLAY TO RESET THE TIME AND DATE. CUSTOMER UNABLE TO VERIFY THE INSULIN PUMP. CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE DEVICE 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 9154852 ↗
• MalfunctionJul 19, 2019Device Difficult to Program or Calibrate; Visual Prompts will not Clear; Device Difficult to Program or Calibrate; Visual Prompts will not Clear

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEIR INSULIN PUMP HAD BUTTON ERROR AND FROZEN DISPLAY. THE CUSTOMER¿S BLOOD GLUCOSE WAS 133 MG/DL AT THE TIME OF INCIDENT. CUSTOMER REPORTED THAT THE TIME CLOCK WAS ADVANCED. CUSTOMER REPORTED THAT THE INSULIN PUMP HAD BUTTON ERROR AND PUSHED EVERY BUTTON AND PULLED THE BATTERY OUT AND BACK AND DID NOT RESET. 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 8806295 ↗
• MalfunctionMay 9, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Power Problem; Patient Device Interaction Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Obstruction of Flow; Power Problem; Patient Device Interaction Problem

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD STICKY BUTTONS. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN. CUSTOMER STATED THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM WITH NO INSULIN DELIVERY ALARMS. THE CUSTOMER STATED THAT THE INSULIN PUMP WAS REJECTING NEW BATTERIES. THE INSULIN PUMP¿S PLASTIC CHIPPING OFF WHEN CHANGING THE RESERVOIR. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8594046 ↗
• MalfunctionMar 4, 2019Connection Problem; Patient Device Interaction Problem; Connection Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT DUCK TAPE WAS PLACED AROUND THE RESERVOIR TO HOLD IT TOGETHER. THE 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 8385507 ↗
• MalfunctionJan 25, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Material Integrity Problem; Power Problem; Patient Device Interaction Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Material Integrity Problem; Power Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD KEYPAD ANOMALY AND DISPLAY ANOMALY. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER REPORTED THAT INSULIN PUMP REJECTED NEW BATTERIES, LOUD GRINDING NOISE WHEN REWINDING AND BUTTONS WERE STICKY AND HARD TO PRESS, SCRATCHES ON PUMP, HARD TO READ SCREEN HAS TO TURN ON. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8276939 ↗
• MalfunctionJan 21, 2019Mechanical Problem; Detachment of Device or Device Component; Mechanical Problem; Detachment of Device or Device Component

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR AND CUSTOMER ALSO STATE THAT DRIVE SUPPORT CAP WAS FLUSH. THE CUSTOMER¿S BLOOD GLUCOSE WAS 288 MG/DL AT THE TIME OF INCIDENT. THE CUSTOMER WAS ADVICE THE INSULIN PUMP WILL NEED TO BE REPLACED. ADVICE TO DISCONTINUE USE OF THE INSULIN PUMP AND REVERT TO 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 8263339 ↗
• InjuryNov 28, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE CUSTOMER PASSED AWAY IN HOSPITAL. THE CUSTOMER WAS HOSPITALIZED ON AND OFF SINCE (B)(6) 2018. THE CAUSE OF DEATH WAS LUNG CANCER. THE CALLER STATED THAT THE CUSTOMER HAD COMPLICATIONS OF LUNG CANCER THAT MAY HAVE LED TO THE CUSTOMER'S PASSING. THE CUSTOMER¿S BLOOD GLUCOSE WAS 500 MG/DL AT THE TIME OF ONE HOSPITALIZATION. THE CUSTOMER WAS NOT WEARING THE INSULIN PUMP AT THE TIME OF DEATH. THE INSULIN PUMP HAD BEEN DISCONNECTED MORE THAN 48 HOURS PRIOR TO PASSING, AS THE HOSPITAL TOOK OVER DIABETES MANAGEMENT AFTER THE HIGH AND UNSTABLE BLOOD GLUCOSE LEVELS. THE CALLER WAS UNSURE IF THE CUSTOMER WAS USING SENSORS. THE CALLER DECLINED TO RETURN THE INSULIN PUMP FOR ANALYSIS.

  Patient problems: Death; Hyperglycemia

  MAUDE report 8109569 ↗
• MalfunctionNov 21, 2018Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THE INSULIN PUMP ALARMED MOTOR ERROR. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER STATED THAT THE DRIVE SUPPORT CAP WAS NORMAL. THE CUSTOMER STATED THAT THE INSULIN PUMP WAS NOT EXPOSED TO HIGH MAGNETIC FIELDS. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND TO REVERT TO THE BACK-UP PLAN. THE INSULIN PUMP WAS RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8096929 ↗
• MalfunctionOct 15, 2018Use of Device Problem; Use of Device Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP REJECTED THE NEW BATTERY. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN. THE CUSTOMER STATED THAT THE INSULIN PUMP HAD UNEXPLAINED NO DELIVERY ALARMS, CRACKS AROUND BATTERY COMPARTMENT AND REJECTED NEW BATTERIES. THE CUSTOMER WAS NOT ASSISTED WITH TROUBLESHOOTING. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7966663 ↗
• MalfunctionSep 20, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP RECEIVED MOTOR ERROR, BUTTON ERRORS, FAILED BATTERY AND FAILED BATTERY. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER REPORTED THAT THE MOTOR ERRORS, NO DELIVERIES, CRACKS IN PUMP, SEVERAL RECENT MOTOR ERRORS, UNEXPLAINED NO DELIVERY, ACT BUTTON WAS STICKING, BATTERY CAP CRACKED AND INSULIN PUMP REJECTED BATTERIES, ALSO SLOWER REWIND PROCESS. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7895631 ↗
• MalfunctionAug 23, 2018Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP ALARMED MOTOR ERROR. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS NOT REPORTED. THE DRIVE SUPPORT CAP WAS PROTRUDED. CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE DEVICE AND REVERT TO A BACKUP PLAN. THE CUSTOMER WAS ADVISED THAT THE DEVICE WOULD BE REPLACED AND AGREED TO RETURN THE PRODUCT FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7811741 ↗
• MalfunctionAug 8, 2018Device Alarm System; Device Alarm System

  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 THAT THE INSULIN PUMP BATTERY LIFE DOES NOT LAST LONG, THERE IS AN ABSENCE OF NO DELIVERY ALARM, AND BUTTONS WERE UNRESPONSIVE,. CUSTOMER DECLINED TROUBLESHOOTING. INSULIN PUMP IS NOT EXPECTED TO RETURN FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7760790 ↗
• MalfunctionAug 7, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  THE CUSTOMER'S MOTHER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP WAS DAMAGE AT THE RESERVOIR COMPARTMENT. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER ALSO STATED THAT THE RESERVOIR LOCK IN PLACE BUT DID NOT HOLD IN PLACE. THE PRODUCT WILL BE RETURNED FOR THE ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7760092 ↗
• MalfunctionJul 9, 2018Break

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEIR INSULIN PUMP WAS DAMAGED. CUSTOMER STATED THE BOTTOM PLASTIC PANEL ON THE MOTOR WHERE THE PISTON IS POPPED OUT WHILE REWINDING. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 164 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND TO REVERT TO THE BACK-UP PLAN. THE INSULIN PUMP WAS RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7672202 ↗
• MalfunctionJul 9, 2018Display or Visual Feedback Problem; Display or Visual Feedback Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THE INSULIN PUMP ALARMED BUTTON ERROR. THE CUSTOMER¿S BLOOD GLUCOSE WAS UNKNOWN AT THE TIME OF INCIDENT. CUSTOMER STATED THAT THE INSULIN PUMP BUTTONS ARE HARD TO PUSH AND SCREEN IS HARD TO READ. THE INSULIN PUMP IS NOT BEING REPLACED OR IS EXPECTED TO RETURN FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7670254 ↗
• MalfunctionJun 13, 2018Moisture Damage

  A CUSTOMER REPORTED VIA PHONE CALL INDICATING THAT THEIR INSULIN PUMP WAS DAMAGED WITH WATER AFTER THE CUSTOMER WENT INTO THE SWIMMING POOL WITH THE DEVICE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 111 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER WAS INFORMED THAT THE INSULIN PUMP NEEDED TO BE REPLACED AND WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND TO REVERT TO THE BACK UP PLAN. THE CUSTOMER SENT THE PRODUCT BACK FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7598813 ↗
• MalfunctionJun 7, 2018Device Operates Differently Than Expected

  THE CUSTOMER'S MOTHER REPORTED VIA PHONE CALL THAT HER DAUGHTER'S INSULIN PUMP HAD A KEYPAD ANOMALY. THE BUTTONS WERE NOT RESPONSIVE. THE INSULIN PUMP ALARMED BATTERY OUT LIMIT. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS NOT REPORTED. CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE DEVICE AND REVERT TO A BACKUP PLAN. THE CUSTOMER WAS ADVISED THAT THE DEVICE WOULD BE REPLACED AND AGREED TO RETURN THE PRODUCT FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7577316 ↗
• MalfunctionDec 22, 2017Device 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 92 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 7143513 ↗
• MalfunctionDec 12, 2017Crack; Physical Property Issue

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEIR INSULIN PUMP WAS DAMAGED. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN. THE CUSTOMER STATES THE 4 CRACKS WHERE THE INSULIN GOES IN, 2 LARGE CHUNKS WHERE THE BATTERY GOES. TROUBLESHOOTING WAS PERFORMED FOR DAMAGE AND NOTICED CRACKED NEAR RESERVOIR COMPARTMENT. THE CUSTOMER STATES RESERVOIR DID NOT LOCK IN PLACE. ADVISED TO DISCONTINUE USE OF THE PUMP AND REVERT TO A BACK-UP PLAN. ADVISED THE PUMP WILL NEED TO BE REPLACED THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7111240 ↗
• MalfunctionNov 9, 2017Break; Detachment Of Device Component

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEIR INSULIN PUMP'S RESERVOIR SCREWS IN HALF OF IT BROKE OFF. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE INSULIN PUMP AND TO REVERT TO THE BACK-UP PLAN. THE INSULIN PUMP IS EXPECTED TO BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7015182 ↗
• MalfunctionOct 26, 2017Failure To Adhere Or Bond

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE RESERVOIR COMPARTMENT WAS PREVENTING THE RESERVOIR FROM SCREWING IN. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL AT THE TIME OF INCIDENT WAS 155 MG/DL. CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE DEVICE AND REVERT TO A BACK-UP PLAN. THE CUSTOMER WAS ADVISED THAT THE DEVICE WOULD BE REPLACED AND AGREED TO RETURN THE INSULIN PUMP FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 6979902 ↗
• MalfunctionOct 24, 2017Crack; Moisture or Humidity Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP WAS EXPOSED TO MOISTURE. THE CUSTOMER¿S BLOOD GLUCOSE AT THE TIME OF THE INCIDENT WAS UNKNOWN. CUSTOMER ALSO REPORTED CRACKS AROUND THE RESERVOIR COMPARTMENT. 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 Known Impact Or Consequence To Patient

  MAUDE report 6971548 ↗

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-1593-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723K
• 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-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-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-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