medical MODERATE Updated 2017-11-29

Medtronic Inc. recalls Medtronic MiniMed(TM) Sure-T(TM) (MMT-862, 862T, 864, 864T,

See all recalls from Medtronic Inc. →

Recalled Product

Medtronic MiniMed(TM) Sure-T(TM) (MMT-862, 862T, 864, 864T, 866, 866T, 874, 874T, 876, 876T, 884, 886, 886T)

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

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

Issued by

FDA

Distribution: Worldwide
Lot/Code Info: Lot Numbers: 5188321 5190185 5190186 5184968 5185467 5185468 5185469 5185470 5188322 5188323 5188324 5188325 5188326 5188327 5188328 5189476 5189477 5189478 5189521 5189522 5190187 5190188 5190189 5191046 5191047 5191355 5192532 5183060 5183061 5187300 5187301 5187556 5187557 5189051 5193052 5188329 5188330 5189053 5189054 5194937 5185690 5187558 5191357 5187559

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Medtronic MiniMed(TM) Sure-T(TM) (MMT-862, →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

Philips North America recalls Philips SmartPath to dStream for 1.5T with MR Elastography (

2026-05-06 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Pa

2026-05-06 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

Philips North America recalls Philips SmartPath to dStream for XR and 3.0T with MR Elastog

2026-05-06 · The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

Medline Industries, LP recalls Medline and Centurion medical procedure kits, containing Med

2026-05-06 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.