Public recall detail

Paradigm and MiniMed 600 and 700 series pumps

2026-02-26

medium
General hospital and personal use Performance
Quick summary

Quick summary: Paradigm and MiniMed 600 and 700 series pumps. Reason: Performance. Category: General hospital and personal use. Date: 2026-02-26.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Paradigm and MiniMed 600 and 700 series pumps. Reason: Performance. Category: General hospital and personal use. Date: 2026-02-26.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandMedtronic Minimed
ProductParadigm and MiniMed 600 and 700 series pumps
IssueMedical devices - Performance
Recall classType II
IdentificationRA-81648

Affected products

ProductMinimed 630g
LotAll lots.
ModelMMT-1714
Serial numberAll lots.
DescriptionMinimed 630g
ProductParadigm 754 Insulin Pump
LotAll lots.
ModelMMT-754
Serial numberAll lots.
DescriptionParadigm 754 Insulin Pump
ProductMinimed 780g Kit
LotAll lots.
ModelMMT-1895
Serial numberAll lots.
DescriptionMinimed 780g Kit
ProductMinimed 670g
LotAll lots.
ModelMMT-1782
Serial numberAll lots.
DescriptionMinimed 670g
ProductParadigm 554 Insulin Pump
LotAll lots.
ModelMMT-554
Serial numberAll lots.
DescriptionParadigm 554 Insulin Pump
ProductMinimed 770g
LotAll lots.
ModelMMT-1891
Serial numberAll lots.
DescriptionMinimed 770g
ProductMinimed 770g
LotAll lots.
ModelMMT-1881
Serial numberAll lots.
DescriptionMinimed 770g
ProductMinimed 670g Kit
LotAll lots.
ModelMMT-1762
Serial numberAll lots.
DescriptionMinimed 670g Kit
ProductMinimed 780g Pump
LotAll lots.
ModelMMT-1885
Serial numberAll lots.
DescriptionMinimed 780g Pump

Issue

As part of the testing for the Alternate Controller Enabled (ACE) device submission, the R&D team tested the Minimed 780g Insulin Pump at elevated and lowered height conditions relative to the infusion site per the engineering test report. The results of the testing showed that there is an unintended over or under delivery of insulin that occurs when the 780g pump is either elevated or lowered relative to the infusion site.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesMedtronic Minimed 18000 Devonshire St., Northridge, California, United States, 91325
Recall date2026-02-19
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-81648
Background{}
CompaniesMedtronic Minimed 18000 Devonshire St., Northridge, California, United States, 91325
AudiencesGeneral public
Source updated2026-02-26

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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