Medtronic Inc.: Medical Device Recall in 2017 - (Recall #: Z-0111-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)

Product Classification:

Class II

Date Initiated: September 10, 2017

Date Posted: November 29, 2017

Recall Number: Z-0111-2018

Event ID: 78125

Reason for Recall:

Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.

Status: Ongoing

Product Quantity: 5,842 units

Code Information:

Lot Numbers: 6211649, 6207537

Distribution Pattern:

Worldwide

Voluntary or Mandated:

Voluntary: Firm initiated