PARADIGM® REAL-time MMT-522NAS (UDI 00613994402097)Recalls & reported problems

Summary

The FDA's MAUDE database contains 85 adverse event reports that list this exact device (DI 00613994402097), received between May 9, 2017 and Jun 19, 2023 — classified as 22 injuries, 63 malfunctions.

The most frequently reported specific device problem is “Device Displays Incorrect Message” (18 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 85 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 19, 2023Break; Obstruction of Flow; Break; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE CUSTOMER REPORTED INSULIN PUMP HAD A CRACK AND NO DELIVERY ALARMS. TROUBLESHOOTING WAS PERFORMED AND FOUND THAT DAMAGE WAS ON THE RESERVOIR AREA AND THE RESERVOIR WAS ABLE TO LOCK IN PLACE. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WILL DISCONTINUE USING THE INSULIN PUMP AND WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17149756 ↗
• MalfunctionJul 5, 2020Patient Device Interaction Problem; Priming Problem; Patient Device Interaction Problem; Priming Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD SHOT OUT INSULIN DURING PRIMING. THE CUSTOMER STATED THAT THE CHUNK OF THE BATTERY PORT WAS MISSING SO THE CAP DID NOT SCREW IN ANYMORE AND THE BATTERY WAS HELD IN WITH TAPE. 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 10231289 ↗
• InjuryMay 18, 2020Obstruction of Flow; Obstruction of Flow

  CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED LOW BLOOD GLUCOSE. THE CUSTOMER BLOOD GLUCOSE LEVEL WAS 45 MG/DL AT THE TIME OF INCIDENT. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING AND DECLINED FOR LOW BLOOD GLUCOSE. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hypoglycemia

  MAUDE report 10064792 ↗
• MalfunctionApr 29, 2020Failure to Cycle; Failure to Cycle

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD COMPROMISED FORCE SENSOR SYSTEM ERROR. CUSTOMER REPORTED THAT THE DRIVE SUPPORT CAP APPEARED TO BE NORMAL. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10009481 ↗
• InjuryApr 17, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED VIA CALL THAT THE CUSTOMER HAD HIGH BLOOD GLUCOSE LEVEL OF 535 MG/DL. CUSTOMER HAD BLOOD GLUCOSE LEVELS OF 478, 409, 346, 435 AND 443 MG/DL. CUSTOMER WAS TREATED WITH MANUAL INJECTION. CUSTOMER WAS USING AUTO MODE. CUSTOMER DID NOT ALLEGE INSULIN PUMP FOR UNDER DELIVERY. CUSTOMER STATED THAT THERE WAS NO AIR BUBBLES AND LEAK. CUSTOMER DID HIGH PRESSURE TEST AND IT WAS PASSED. CUSTOMER WAS USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE LEVEL EVENT. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9974875 ↗
• MalfunctionApr 16, 2020Mechanical Problem; Mechanical Problem

  CUSTOMER REPORTED VIA PHONE CALL THE INSULIN PUMP HAD KEYPAD ISSUE. CUSTOMER BLOOD GLUCOSE AT THE TIME OF INCIDENT WAS UNKNOWN. TROUBLESHOOTING WAS NOT PERFORMED. THE INSULIN PUMP WILL BE RETURNING FOR ANALYSIS

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9966947 ↗
• MalfunctionApr 1, 2020Mechanical Problem; Detachment of Device or Device Component; Mechanical Problem; Detachment of Device or Device Component

  INFORMATION INDICATED BY MEDTRONIC THAT THE INSULIN PUMP HAD A MOTOR ERROR. CUSTOMER STATED THAT 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 Consequences Or Impact To Patient

  MAUDE report 9909773 ↗
• MalfunctionMar 4, 2020Mechanical Problem; Obstruction of Flow; Mechanical Problem; Obstruction of Flow

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD REWIND ANOMALY AND NO DELIVERY ALARMS. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WAS RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9784571 ↗
• InjuryFeb 12, 2020Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event; Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event

  THE CUSTOMER¿S HUSBAND REPORTED VIA PHONE CALL THAT CUSTOMER EXPERIENCED HIGH BLOOD GLUCOSE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 487 MG/DL AT THE TIME OF INCIDENT. THE CUSTOMER DID NOT EXPERIENCED SYMPTOMS DUE TO HIGH BLOOD GLUCOSE. THE CUSTOMER TREATED HIGH BLOOD GLUCOSE WITH BOLUS. CUSTOMER HAD BEEN USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE EVENT. THE CUSTOMER DID ALLEGE UNDER DELIVERY ON INSULIN PUMP BECAUSE BLOOD GLUCOSE VALUE DID NOT GO DOWN. THE INSULIN PUMP PASSED HIGH PRESSURE TEST AND DISPLACEMENT TEST. CUSTOMER REPORTED INSULIN PUMP WAS NOT WORN DURING A MEDICAL PROCEDURE. THE CUSTOMER STATED THAT THE BASAL RATE AND BOLUS WIZARD WAS PROGRAMMED ACCURATELY. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9699142 ↗
• InjuryFeb 10, 2020Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY WERE EXPERIENCING HIGH BLOOD GLUCOSE. BLOOD GLUCOSE LEVEL AT TIME OF INCIDENT WAS 400 MG/DL. CUSTOMER DECIDED TO TAKE A MANUAL SHOT. CUSTOMER STATED THAT THEY DID NOT FEEL OKAY TO TROUBLESHOOTING. CUSTOMER STATED THAT THE DRIVE SUPPORT CAP APPEARS NORMAL. CUSTOMER STATED THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER WAS ABLE TO SUCCESSFULLY CLEAR THE ALARM. CUSTOMER WAS ABLE TO COMPLETE INSULIN PUMP REWIND. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9686977 ↗
• MalfunctionFeb 4, 2020Display or Visual Feedback Problem; Display or Visual Feedback Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP'S SCREEN WENT DARK SUDDENLY. TROUBLESHOOTING WAS DONE FOR PARTIAL DISPLAY. THE CUSTOMER STATED THAT THE INSULIN PUMP WAS NEITHER DROPPED NOR BUMPED. 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 9669041 ↗
• MalfunctionJan 30, 2020Mechanical Problem; Power Problem; Patient Device Interaction Problem; Mechanical Problem; Power Problem; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM. CUSTOMER STATED THAT THERE WAS CRACK ON SIDE OF INSULIN PUMP. 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 9646295 ↗
• MalfunctionJan 28, 2020Mechanical Problem; Detachment of Device or Device Component; Mechanical Problem; 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 NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9640294 ↗
• MalfunctionJan 17, 2020Electrical /Electronic Property Problem; Battery Problem; Power Problem; Electrical /Electronic Property Problem; Battery Problem; Power Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD EXTERNAL FLASH ERROR ALARM. CUSTOMER ALSO REPORTED THAT HE INSULIN PUMP HAD BATTERY OUT LIMIT ALARM, DIMINISHED BATTERY LIFE, ERASED SETTINGS WHEN CHANGING BATTERIES AND REJECTED A NEW BATTERY. TROUBLESHOOTING WAS SKIPPED. THE INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9599815 ↗
• MalfunctionDec 27, 2019Mechanical Problem; Use of Device Problem; Mechanical Problem; Use of Device Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM THRICE. THE CUSTOMER'S BLOOD GLUCOSE VALUE WAS UNKNOWN. CUSTOMER STATED THEY HAD TO RESET DATE AND TIME AND SOME SETTINGS ON BATTERY AND ALSO CUSTOMER DECLINED TROUBLESHOOTING. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9522582 ↗
• MalfunctionDec 9, 2019Mechanical Problem; Loss of Data; Patient Device Interaction Problem; Mechanical Problem; Loss of Data; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE THAT THE INSULIN PUMP HAD UNEXPECTED RESTART ALARM. CUSTOMER¿S BLOOD GLUCOSE WAS MORE THAN 200 MG/DL AT THE TIME OF INCIDENT. CUSTOMER STATED THAT THE PISTON WAS NOT STOP MOVING FORWARD UNTIL IT PUSHES ALL THE INSULIN OUT. CUSTOMER STATED THAT THE RESERVOIR AND BATTERY COMPARTMENT WAS CRACKED. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE PUMP AND REVERT TO BACKUP PLAN PER HEALTHCARE PROFESSIONAL INSTRUCTIONS. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9436840 ↗
• MalfunctionDec 6, 2019Connection Problem; Patient Device Interaction Problem; Connection Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP WAS DAMAGED AND THE RUBBER RING WAS REMOVED FROM THE RESERVOIR COMPARTMENT CAUSING THE RESERVOIR NOT TO LOCK IN PLACE. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 161 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 BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9422304 ↗
• MalfunctionNov 19, 2019Use of Device Problem; Insufficient Device Problem Information; Use of Device Problem; Insufficient Device Problem Information

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP BATTERY WAS DIED AND SETTINGS WERE LOST . 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 9344313 ↗
• MalfunctionNov 15, 2019Mechanical Problem; Device Difficult to Program or Calibrate; Power Problem; Patient Device Interaction Problem; Mechanical Problem; Device Difficult to Program or Calibrate; Power Problem; Patient Device Interaction Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERRORS AND BUTTONS DID NOT RESPOND. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER REPORTED THAT THE INSULIN PUMP HAD CRACKS ON CASING AND REJECTS BATTERIES. THE INSULIN PUMP WILL NOT BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9328470 ↗
• MalfunctionNov 1, 2019Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD MOTOR ERROR ALARM. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 300 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER REPORTED THAT THEY WERE HIGH WHEN THEY CHECKED THE BLOOD GLUCOSE 3 DAYS AGO AND HAD TO USE THE MANUAL INSULIN. THE CUSTOMER REPORTED THAT WAS BECAUSE OF THE MOTOR ERROR THEY WERE GETTING BUT THEY FEELING OKAY BECAUSE THE PUMP WAS WORKING. THE CUSTOMER REPORTED MOTOR FAILED. THE CUSTOMER REPORTED THAT IT GRADUALLY HAPPENED OVER THE LAST YEAR AND INCREASE GETTING THE ALERT OVER THE LAST 2 MONTHS. THE CUSTOMER REPORTED THAT THEY WERE ABLE TO CLEAR THE ALARMS AND WERE ABLE TO COMPLETE REWIND. THE INSULIN PUMP PASSED THE SELF TEST BUT IT KEPT HAPPENING THE PAST 2 MONTHS AND HAD TO TURN OFF THE INSULIN PUMP FOR 2 DAYS. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 9264892 ↗
• MalfunctionOct 16, 2019Priming Problem; Priming Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD INSULIN SQUIRTING OUT DURING THE MANUAL PRIME PROCESS. THE CUSTOMER'S BLOOD GLUCOSE VALUE WAS 327 MG/DL. THE CUSTOMER WAS ABLE TO COMPLETE THE REWIND. CUSTOMER STATED THEY DID NOT RECEIVED 2ND SERIES OF BEEPS NOR DID NUMBERS APPEARED ON THE SCREEN. THE DEVICE WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9195654 ↗
• MalfunctionSep 24, 2019No Display/Image; No Display/Image

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD BLANK DISPLAY. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 135 MG/DL. THE CUSTOMER REPORTED THAT THE DISPLAY WAS NOT BLANK LESS THAN 30 SECONDS AND DID NOT RETURN.. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING AND CUSTOMER REPORTS DISPLAY WAS BLANK CURRENTLY. THE CUSTOMER REMOVES THE BATTERY AND STATED THE INSERT BATTERY ALARM DID NOT DISPLAY ON THE INSULIN PUMP SCREEN. CUSTOMER STATES THE CONTACT ON THE BATTERY CAP WAS NEITHER MISSING NOR DAMAGE. CUSTOMER STATES BATTERY COMPARTMENT WAS NEITHER DAMAGED NOR CORRODED. CUSTOMER STATES THE SPRING WAS NEITHER DAMAGED NOR CORRODED. CUSTOMER STATES THE DISPLAY DID NOT RETURN AFTER INSULIN PUMP RESTART. 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 9108772 ↗
• MalfunctionSep 10, 2019Adverse Event Without Identified Device or Use Problem; Power Problem; Intermittent Communication Failure; Adverse Event Without Identified Device or Use Problem; Power Problem; Intermittent Communication Failure

  CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD REPLACE BATTERY NOW ALARM. CUSTOMER'S BLOOD GLUCOSE VALUE WAS 149 MG/DL AT THE TIME OF THE INCIDENT. THE CUSTOMER WAS ASSISTED WITH TROUBLESHOOTING. CUSTOMER STATED THAT THE NEW BATTERY DID NOT RESOLVE THE ISSUE. ADVISED THE INSULIN PUMP WILL NEED TO BE REPLACED. ADVISED TO DISCONTINUE USE OF 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 8978857 ↗
• MalfunctionAug 19, 2019Display or Visual Feedback Problem; Display or Visual Feedback Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP HAD DARK IMAGE ON THEE MIDDLE OF HER SCREEN. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN AT THE TIME OF THE INCIDENT. THE CUSTOMER STATED THAT DISPLAY WAS FLASHING. ADVISED THE PUMP WILL NEED TO BE REPLACED. ADVISED TO DISCONTINUE USE OF THE PUMP AND REVERT TO A BACK-UP PLAN. TROUBLESHOOTING WAS PERFORMED. INSULIN PUMP WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8905237 ↗
• MalfunctionAug 14, 2019No Display/Image; Mechanical Problem; Visual Prompts will not Clear; Obstruction of Flow; No Apparent Adverse Event; No Display/Image; Mechanical Problem; Visual Prompts will not Clear; Obstruction of Flow; No Apparent Adverse Event

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THE INSULIN PUMP WAS UNRESPONSIVE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS UNKNOWN TIME OF THE INCIDENT. CUSTOMER ALSO REPORTED OCCASIONAL GRINDING NOISE DIFFERENT FROM THE NORMAL REWIND NOISE AND RANDOM NO DELIVERY ALARMS WAS FOUND. THE INSULIN PUMP WILL NOT BE RETURN FOR ANALYSIS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8891814 ↗

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-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-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-1594-2020 · Jun 27, 2019 · Open, Classified
  Medtronic MiniMed Paradigm Insulin pump, model number MMT-723
• 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-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