Medtronic Recalls
157 recalls on record · November 11, 2015 to May 6, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 11, 2018Medical DevicesFDA
Medtronic Inc. recalls Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754
Hazard: The MiniMed Paradigm Veo insulin pump has an error that impacts the Arabic language translation.This translation error occurs in the Predictive Alerts setting screen, which allows user to program alerts that will sound if users are predicted to reach their pre-set low or high sensor glucose values.
April 4, 2018Medical DevicesFDA
Medtronic Inc recalls 6F Taiga Guiding Catheter
Hazard: Complaints regarding 6F Taiga guide catheter tip detachment and/or tip splitting.
February 28, 2018Medical DevicesFDA
Medtronic Inc. recalls Medtronic CareLink iPro Therapy Management Software, MMT-7340 The CareLink iPro Therapy Management Software (model, M
Hazard: Due to a time conversion error, data uploaded from the iPro(TM)2 recorder to the CareLink iPro software using the new CareLink iPro Uploader feature may result in incorrect reports. This pertains only to reports generated between September 23, 2017 and September 27, 2017 that used the new CareLink iPro Uploader feature.
December 6, 2017Medical DevicesFDA
Medtronic Inc. recalls Everflex Self-Expanding Peripheral Stent with Entrust Delivery System Intended to improve luminal diameter in the trea
Hazard: Stent length on the label may not match the length of the stent itself.
November 29, 2017Medical DevicesFDA
Medtronic Inc. recalls Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)
Hazard: Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
November 29, 2017Medical DevicesFDA
Medtronic Inc. recalls Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T, 965
Hazard: Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
November 29, 2017Medical DevicesFDA
Medtronic Inc. recalls Medtronic MiniMed(TM) Sure-T(TM) (MMT-862, 862T, 864, 864T, 866, 866T, 874, 874T, 876, 876T, 884, 886, 886T)
Hazard: Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
November 29, 2017Medical DevicesFDA
Medtronic Inc. recalls Medtronic MiniMed(TM) Silhouette(TM) (MMT-377, 377T, 378, 378T, 384, 384T, 368, 368T, 381, 381T, 382, 382T, 383, 383T)
Hazard: Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
November 29, 2017Medical DevicesFDA
Medtronic Inc. recalls Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)
Hazard: Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
June 28, 2017Medical DevicesFDA
Medtronic Inc. recalls MiniMed 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760.
Hazard: Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
June 28, 2017Medical DevicesFDA
Medtronic Inc. recalls MiniMed 640G Insulin Infusion Pump, Catalog No. MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1551, MMT-1751, MMT-1552, MM
Hazard: Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
June 28, 2017Medical DevicesFDA
Medtronic Inc. recalls MiniMed 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755.
Hazard: Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
June 28, 2017Medical DevicesFDA
Medtronic Inc. recalls MiniMed 620G Insulin Infusion Pump, Catalog No. MMT-1510, MMT-1710, MMT-1550, MMT-1750.
Hazard: Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
June 21, 2017Medical DevicesFDA
Medtronic recalls SCHRITTMACHER ANGIO X3; Item Number: 4045255423347
Hazard: Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
June 21, 2017Medical DevicesFDA
Medtronic recalls CUSTOM SUTURE PACK; Item Number: US1540 and US1614
Hazard: Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
June 21, 2017Medical DevicesFDA
Medtronic recalls USPACK-SUTURE KIT; Item Number: US1672
Hazard: Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
June 21, 2017Medical DevicesFDA
Medtronic recalls Best Practice Kit, Item Numbers: 00Z2064, 00Z2150, 00Z2190, 00Z2192, 00Z2211, 00Z2212, 00Z2216, 00Z2217, 00Z2312
Hazard: Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
June 21, 2017Medical DevicesFDA
Medtronic recalls Sutures. BIOSYN: BIOSYN 4/0 18" VIOLET CV-25 DT, Item Number: GMJ34M
Hazard: Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
June 21, 2017Medical DevicesFDA
Medtronic recalls Sutures. ENDO STITCH: ENDO STITCH POLYSORB 0 48" U/D DLU SU, Item Number: 170056; ENDO STITCH POLYSORB 0 48" VIO DLU SU
Hazard: Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
June 21, 2017Medical DevicesFDA
Medtronic recalls Sutures. MAXON: MAXON 4/0 5X18" GREEN CV-24 D-TACH; Item Number: 8886621933; MAXON 5/0 5X18 GR CV-23 D-TACH; Item Numbe
Hazard: Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
June 21, 2017Medical DevicesFDA
Medtronic recalls Sutures. POLYSORB: POLSORB 0 18 U/D PRECUT 126R, Item Number: L4; POLSORB 0 18 VIO PRECUT 226T; Item Number: L14; POLSO
Hazard: Potential for an incomplete seal on the inner package, which may result in premature degradation of the suture material.
May 10, 2017Medical DevicesFDA
Medtronic Inc. recalls MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2.6 and below are affected. Catalog Numbers for these
Hazard: Medtronic has identified a software anomaly that can prevent the internal battery of the pump from charging. When the software anomaly occurs it leads to battery depletion and pump shutdown.
March 22, 2017Medical DevicesFDA
Medtronic recalls BNX Fine Need Aspiration System (22GA); Material/Part#: DSN-22-01
Hazard: Handle may break during use.
March 22, 2017Medical DevicesFDA
Medtronic recalls SharkCore LG Fine Needle Biopsy System (19GA); Material/Part#: DSL-19-01
Hazard: Handle may break during use.
March 22, 2017Medical DevicesFDA
Medtronic recalls SharkCore Fine Needle Biopsy System (25GA); Material/Part#: DSC-25-01
Hazard: Handle may break during use.
March 22, 2017Medical DevicesFDA
Medtronic recalls SharkCore Fine Needle Biopsy System (22 GA); Material/Part #s: DSC-22-01
Hazard: Handle may break during use.
March 22, 2017Medical DevicesFDA
Medtronic recalls BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01
Hazard: Handle may break during use.
December 28, 2016Medical DevicesFDA
Medtronic Inc recalls ev3, PowerCross .018 OTW PTA Dilatation Catheter, Sterile EO. The PowerCross .018 OTW PTA Dilatation Catheter is intend
Hazard: Medtronic identified an issue with specific models and lots of the PowerCross .018 Over the Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter. During an unrelated manufacturing inspection of scrapped products, an out of specification condition was observed. The catheter outer shafts were pinched and deformed at the proximal balloon bond. Bench testing of affected devices showed that this resulted in either the inability to inflate the device, a slow deflation, or the inability to deflate the device post expansion.
December 28, 2016Medical DevicesFDA
Medtronic recalls Best Practices kits containing certain production lots of Clearify Visualization System Item Code: 21-345 Intended to
Hazard: Product sterility is compromised due to breach of the sterile barrier
December 28, 2016Medical DevicesFDA
Medtronic recalls Covidien Clearify Visualization System Item Code: 21-345 Intended to be used prior to and during endoscopic and lapar
Hazard: Product sterility is compromised due to breach of the sterile barrier