MiniMed® 630G MMT-1715KR (UDI 00763000173036)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1,195 adverse event reports that list this exact device (DI 00763000173036), received between Jan 17, 2019 and Jun 25, 2025 — classified as 9 deaths, 507 injuries, 679 malfunctions.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (201 reports).

10 other recalls cover devices cleared under the same FDA submission (P150001); 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 1,195 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 25, 2025Break; Battery Problem; Break; Battery Problem

  IT WAS REPORTED TO MEDTRONIC MINIMED THAT THE CUSTOMER EXPERIENCED RAPID BATTERY DEPLETION, WITH THE BATTERY LASTING ONLY 6 TO 7 DAYS. THE CUSTOMER ALSO REPORTED A CRACK ON THE INSULIN PUMP'S CLIP RAILS. THE CUSTOMER REPORTED NO ADVERSE EVENT. THE EVENT INVOLVED PRODUCT(S) MMT-1715KR. TROUBLESHOOTING WAS PERFORMED THAT INCLUDED CHECKING THE BATTERY CAP FOR CORROSION OR DAMAGE AND REVIEWING THE PUMP'S CONDITION, BUT THE ISSUE PERSISTED. THE CUSTOMER WAS ADVISED TO DISCONTINUE USE OF THE PUMP, REVERT TO THE BACKUP PLAN PER HEALTHCARE PROFESSIONAL'S INSTRUCTIONS, AND FOLLOW PUMP CARE BEST PRACTICES. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22325877 ↗
• MalfunctionAug 2, 2022Break; Patient Device Interaction Problem; Break; Patient Device Interaction Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE RETAINER RING WAS DAMAGED. THE RESERVOIR WAS ABLE TO LOCK IN THE PLACE. CUSTOMER STATED THAT THE INSULIN PUMP HAD NEITHER BEEN BUMPED NOR DROPPED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE CUSTOMER WILL DISCONTINUE TO USE THE DEVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15146248 ↗
• MalfunctionJul 25, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE CUSTOMER COULD NOT READ . NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE INSULIN PUMP WAS RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15093488 ↗
• DeathJul 19, 2022Adverse 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 IN HOSPITAL. THE CUSTOMER WAS HOSPITALIZED ON (B)(6) 2020. THE CAUSE OF DEATH WAS STROKE. THE CALLER STATED THAT THE CUSTOMER HAD HEART SURGERY FOUR YEARS AGO THAT MAY HAVE LED TO THE CUSTOMER'S PASSING. THE CUSTOMER¿S BLOOD GLUCOSE AT THE TIME OF DEATH WAS UNKNOWN. THE CUSTOMER WAS NOT WEARING THE INSULIN PUMP AT THE TIME OF DEATH. IT WAS UNKNOWN IF AUTO MODE ON THE INSULIN PUMP WAS ACTIVE AND AUTOMATICALLY ADJUSTING INSULIN DELIVERY DURING THE EVENT. THE INSULIN PUMP HAD BEEN DISCONNECTED ONE DAY PRIOR TO PASSING. THE CALLER RETURNED THE INSULIN PUMP FOR ANALYSIS.

  Patient problems: Stroke/CVA

  MAUDE report 15049174 ↗
• MalfunctionJul 18, 2022Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED VIA PHONE CALL THAT THEY EXPERIENCED HIGH BLOOD GLUCOSE. THE CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 300 MG/DL. THE CUSTOMER TREATED HIGH BLOOD GLUCOSE WITH INSULIN PUMP. THE CUSTOMER HAD BEEN USING INSULIN PUMP SYSTEM WITHIN 48 HOURS OF REPORTED HIGH BLOOD GLUCOSE EVENT. THE CUSTOMER WAS NEITHER IN THE EMERGENCY ROOM, NOR ADMITTED INTO HOSPITAL AS A RESULT OF HIGH BLOOD GLUCOSE. THE CUSTOMER DID ALLEGE UNDER DELIVERY ON INSULIN PUMP. TROUBLESHOOTING WAS PERFORMED. NO FURTHER PATIENT COMPLICATIONS WERE REPORTED. FRN-MMT-332-RSVR, UNOMED INF SET MMT-397.

  Patient problems: Hyperglycemia; Urinary Frequency / Polyuria

  MAUDE report 15042501 ↗
• DeathJul 18, 2022Adverse 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 COUSIN REPORTED VIA PHONE CALL THAT THE CUSTOMER HAD PASSED AWAY ON (B)(6) 2019. THE CAUSE OF THE DEATH WAS SEVERE PNEUMONIA. THE INSULIN PUMP WAS NOT WORN AT THE TIME OF PASSING. THE INSULIN PUMP WAS RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 15039868 ↗
• DeathJul 18, 2022Material Integrity Problem; Adverse Event Without Identified Device or Use Problem; Material Integrity Problem; Adverse Event Without Identified Device or Use Problem

  COMPLAINTS TEXT 07/14/2020 13:42:58 DIAZL76 TRACKING NUMBER: (B)(4). SERVICE: UPS NEXT DAY AIRLABEL DELIVERY METHOD: 3 UPS PICKUP ATTEMPTS. COMPLAINTS TEXT 06/27/2020 07:35:31 MATTEC3 I MARKED THE ACCOUNT INACTIVE/DECEASED (WHILE OPTING OUT OF ALL COMMUNICATIONS) AS WELL AS VOIDED THE MEDTRONIC DEVICE/PUMP WARRANTY. WARRANTY END DATE WILL REFLECT (B)(6) 2020 DATE OF CUST PASSING PER REPORT. COMPLAINTS TEXT 06/26/2020 12:50:24 ERP_RFC_USER RELATED SVN (B)(4). COMPLAINTS TEXT 06/26/2020 12:40:28 ERP_RFC_USER RELATED SVN (B)(4). COMPLAINTS TEXT 06/26/2020 12:39:34 ERP_RFC_USER RELATED SVN (B)(4). COMPLAINTS TEXT 06/26/2020 12:34:12 SIAPNA2 INITIAL NOTES: CUST STATED THAT SHE IS CALLING TO CHECK ON HOW TO SEND THE PUMP BACK INQUIRED WHAT LED UP TO THE COMPLAINT. CUSTOMER RESPONSE: PT PASSED AWAY DECEASED REPORTING PER (B)(4). WHAT LED UP TO EVENT: CHRONIC RESPIRATORY PROBLEM . FIRST AND LAST NAME OF PERSON REPORTING EVENT: (B)(6). BEST PHONE NUMBER TO REACH PERSON REPORTING EVENT: (B)(6). RELATIONSHIP OF PERSON REPORTING EVENT TO THE DECEASED: SPOUSE . REPORTING PARTY IS AWARE OF THE DECEASED EVENT DETAILS. DATE OF CUSTOMER PASSING: (B)(6) 2020. CAUSE OF CUSTOMER PASSING AS INDICATED B

  Patient problems: Unspecified Respiratory Problem

  MAUDE report 15039745 ↗
• MalfunctionJul 18, 2022Patient Device Interaction Problem; Patient Device Interaction Problem

  MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS AN ALLEGATION OF HYPERGLYCEMIA AS A RESULT OF THIS EVENT.

  Patient problems: Hyperglycemia

  MAUDE report 15039678 ↗
• DeathJul 18, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  COMPLAINTS TEXT 02/01/2020 06:57:45 ERP_RFC_USER RELATED SVN (B)(4). COMPLAINTS TEXT 02/01/2020 06:57:41 ERP_RFC_USER RELATED SVN (B)(4). COMPLAINTS TEXT 02/01/2020 06:57:32 SANCHK29 I MARKED THE ACCOUNT INACTIVE/DECEASED AS WELL AS VOIDED THE DEVICE/PUMP WARRANTY TO REFLECT THE END DATE AS THE DATE THE NOTIFICATION WAS RECEIVED OF CUSTOMERS PASSING (01/31/2020). I OPTED OUT OF MARKETING/ACCOUNT COMM. PREF. COMPLAINTS TEXT 01/31/2020 09:10:56 ERP_RFC_USER RELATED SVN (B)(4). COMPLAINTS TEXT 01/31/2020 09:10:45 MARIGM2 INITIAL NOTES: (B)(6) ((B)(6)/HUSBAND) CALLED IN RECEIVED INVOICE AND CALLING TO REPORT PASSING OF THE PATIENT. INQUIRED WHAT LED UP TO THE COMPLAINT. CUSTOMER RESPONSE: HUSBAND CALLING TO REPORT THE DEATH OF THE PATIENT. DECEASED REPORTING PER (B)(4). FIRST AND LAST NAME OF PERSON REPORTING EVENT: (B)(6). BEST PHONE NUMBER TO REACH PERSON REPORTING EVENT: (B)(6). RELATIONSHIP OF PERSON REPORTING EVENT TO THE DECEASED: SPOUSE. REPORTING PARTY IS AWARE OF THE DECEASED EVENT DETAILS. DATE OF CUSTOMER PASSING: (B)(6) 2019. CAUSE OF CUSTOMER PASSING AS INDICATED BY REPORTING PARTY: RECOVERING FROM SURGERY BECAUSE SHE HAD FALLEN AND HAS BROKEN BONE. LOCATION OF CUSTOMER¿S

  Patient problems: Bone Fracture(s); Fall

  MAUDE report 15039549 ↗
• DeathJul 18, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  COMPLAINTS TEXT 06/15/2020 17:24:00 ALBANA5 INITIAL NOTES: CUSTOMER RECEIVED ANOTHER ENVELOPE FOR RETURNING THE PUMP. THE PUMP WAS ALREADY RETURNED LAST WEEK. CUSTOMER ONLY USED THE BOX AND THE UPS STICKER, NO LETTER ENVELOPE WAS USED. PUMP STILL SHOWS IN NOT RECEIVED YET INQUIRED WHAT LED UP TO THE COMPLAINT. CUSTOMER RESPONSE: CUSTOMER RECEIVED ANOTHER ENVELOPE FOR RETURNING THE PUMP. THE PUMP WAS ALREADY RETURNED LAST WEEK. CUSTOMER ONLY USED THE BOX AND THE UPS STICKER, NO LETTER ENVELOPE WAS USED. PUMP STILL SHOWS IN NOT RECEIVED YET CUSTOMER'S OUTCOME PERTAINING TO THE COMPLAINT: ADVISED CUSTOMER THE LETTER ENVELOPE WAS SUPPOSED TO BE USED TO RETURN THE PUMP. THE BOX WAS SUPPOSED TO GO IN THE LETTER ENVELOPE WHILE THE UPS STICKER WAS MEANT TO BE PLACED OUTSIDE THE LE. SHIP: NOTHING / RETURN: NOTHING. COMPLAINTS TEXT 06/08/2020 08:41:46 MOLLAA1 I MARKED THE ACCOUNT INACTIVE/DECEASED (WHILE OPTING OUT OF ALL COMMUNICATIONS) AS WELL AS VOIDED THE MEDTRONIC DEVICE WARRANTY. SEE S/O TRANSACTION (B)(4) AND THE UPS CAMPUSSHIP RETURN REQUEST FOR THE RETURN OF THE REFERENCED DEVICE TO MEDTRONIC. TRACKING NUMBER: (B)(4) SERVICE: UPS NEXT DAY AIR LABEL DELIVERY METHOD: PRINT AND MAIL RE

  Patient problems: Heart Failure/Congestive Heart Failure

  MAUDE report 15038554 ↗
• DeathJul 15, 2022Adverse 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 IN HOSPITAL. THE CUSTOMER WAS HOSPITALIZED ON (B)(6) 2020 DUE TO HEART FAILURE. THE CAUSE OF DEATH WAS HEART FAILURE. THE CUSTOMER WAS NOT WEARING THE INSULIN PUMP AT THE TIME OF DEATH. IT IS UNKNOWN IF THE CALLER WILL RETURN THE INSULIN PUMP FOR ANALYSIS. FRN-MMT-332-RSVR, UNOMED INF SET.

  Patient problems: Heart Failure/Congestive Heart Failure

  MAUDE report 15026930 ↗
• MalfunctionJul 13, 2022No Apparent Adverse Event; Appropriate Device Problem Term/Code Not Available; No Apparent Adverse Event; Appropriate Device Problem Term/Code Not Available

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP WAS AUTOMATICALLY SUSPENDING DELIVERY EVEN WHEN THE CUSTOMER WAS NOT ON LOW. TROUBLESHOOTING WAS PERFORMED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WILL BE RETURNED FOR ANALYSIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14998587 ↗
• MalfunctionJul 13, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE INSULIN PUMP WAS NOT DELIVERING INSULIN. CUSTOMER DID NOT RECEIVED ANY ALARM. THE BLOOD GLUCOSE TESTER WAS REPLACED BUT STILL THE ISSUE PERSISTED. TROUBLESHOOTING WAS PERFORMED. NO HARM REQUIRING MEDICAL INTERVENTION WAS REPORTED. THE PRODUCT WILL BE RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 14998583 ↗
• MalfunctionJul 12, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  INFORMATION RECEIVED BY MEDTRONIC INDICATED THAT THE CUSTOMER EXPERIENCED HYPERGLYCEMIA. CUSTOMER'S BLOOD GLUCOSE WAS BETWEEN 200-300 MG/DL. CUSTOMER WAS TREATED WITH INSULIN PUMP. THE INSULIN PUMP WAS RETURNED FOR ANALYSIS.

  Patient problems: Hyperglycemia

  MAUDE report 14984765 ↗
• MalfunctionJul 12, 2022Adverse 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

  MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: Hyperglycemia; Hypoglycemia

  MAUDE report 14984717 ↗
• MalfunctionJul 8, 2022Break

  MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14953968 ↗
• MalfunctionJul 8, 2022Break

  MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14953744 ↗
• MalfunctionJul 8, 2022Break

  MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14953692 ↗
• MalfunctionJul 8, 2022Break

  MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14953150 ↗
• MalfunctionJul 7, 2022Break

  MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14952538 ↗
• MalfunctionJul 7, 2022Break

  MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14951892 ↗
• MalfunctionJul 7, 2022Battery Problem

  MEDTRONIC RECEIVED INFORMATION THAT CHARGE/BATTERY LASTS LESS THAN EXPECTED OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14951484 ↗
• MalfunctionJul 6, 2022Break; Material Integrity Problem; Material Integrity Problem

  MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14936109 ↗
• MalfunctionJul 4, 2022Obstruction of Flow

  MEDTRONIC RECEIVED INFORMATION THAT NO DELIVERY/OCCLUSION ALARM DURING THERAPY OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14906834 ↗
• MalfunctionJul 4, 2022Break

  MEDTRONIC RECEIVED INFORMATION THAT DAMAGE (PHYSICAL OR COSMETIC) OCCURRED. THERE WAS NO ADVERSE IMPACT OR CONSEQUENCE REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14905654 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P150001. One submission often covers many models, so check the product and lot details in each record.

• Z-1740-2026 · Feb 13, 2026 · Open, Classified
  MiniMed 630G Insulin Pump (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
• Z-1259-2025 · Jan 31, 2025 · Open, Classified
  MiniMed insulin pump, REF: 630G (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
• Z-0001-2025 · Jul 31, 2024 · Open, Classified
  MiniMed 630G Insulin Pump, REF: MMT-1515, MMT-1714, MMT-1715, MMT-1754, MMT-1755; MiniMed 700G Insulin Pump, REF: MMT-1800, MMT-1801, MMT-1805, MMT-1850, MMT-1851
• Z-0193-2023 · Sep 20, 2022 · Open, Classified
  Insulin Pump/Model: MiniMed 630G/ MMT-1715, MMT-1755, MMT-1754; MiniMed 670G/ MMT-1780, MMT-1781, MMT-1782, MMT-1760, MMT-1761, MMT-1762, MMT-1740, MMT-1741, MMT-1742
• Z-0855-2022 · Jan 27, 2022 · Open, Classified
  MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782; MiniMed 770G: MMT-1880, MMT-1881
• Z-0517-2021 · Apr 30, 2020 · Open, Classified
  MiniMed 630G with SmartGuard, insulin pump, Ref/Model # MMT-1754K, MMT-1714K, MMT-1755K - Product Usage: intended for continuous delivery of basal insulin (at user selectable rate
• Z-0955-2020 · Nov 21, 2019 · Open, Classified
  Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and Canada Version Only
• Z-0683-2019 · Oct 3, 2018 · Open, Classified
  Medtronic MiniMed 630G 6025805-003_C, Rx Only Medtronic MiniMed 670G 6025805-005_B, Rx Only Medtronic MiniMed 640G (International)
• Z-2603-2017 · May 8, 2017 · Terminated
  MiniMed 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755.
• Z-2602-2017 · May 8, 2017 · Terminated
  MiniMed 620G Insulin Infusion Pump, Catalog No. MMT-1510, MMT-1710, MMT-1550, MMT-1750.