PUMP MMT-1780KPK 670G PATHWAY BLACK MG
by MEDTRONIC PUERTO RICO OPERATIONS CO.
The PUMP MMT-1780KPK 670G PATHWAY BLACK MG by MEDTRONIC PUERTO RICO OPERATIONS CO. has a safety score of 28 out of 100, placing it in the high-risk category. Based on FDA MAUDE data, there have been 224,336 adverse event reports including 474 deaths since its introduction in 2015. With an estimated 0 units in use, the incident rate is 0 per 10,000 units. It ranks #234 out of 234 devices in the Infusion Pumps category.
Should you be concerned? A safety score of 28/100 is a serious red flag. 224,336 adverse events including 474 deaths have been reported. The incident rate of 0 per 10,000 units is significantly higher than comparable devices. We strongly recommend discussing alternatives with your healthcare provider before proceeding.
No recalls have been issued for this device — a positive indicator of manufacturing quality and design safety. On the market since 2015, this device has 11 years of real-world data — enough for long-term safety patterns to emerge.
Questions to Ask Your Doctor About the PUMP MMT-1780KPK 670G PATHWAY BLACK MG
1. “What alternatives exist to the PUMP MMT-1780KPK 670G PATHWAY BLACK MG?”This device ranks #234 of 234 in the Infusion Pumps category. There are 233 devices with better safety scores — ask if any are appropriate for your case.
2. “How many of these have you personally implanted or used?”Surgeon experience with a specific device significantly impacts outcomes. Higher procedure volume correlates with fewer complications.
3. “What are the specific risks for my case?”Overall adverse event rates (0 per 10,000) are averages — your individual risk depends on age, health conditions, and anatomy.
4. “Is there a newer generation of this device available?”The PUMP MMT-1780KPK 670G PATHWAY BLACK MG has been on the market since 2015 (11 years). Newer versions may have improved safety profiles based on lessons from earlier models.
Adverse Events
Total reports filed with FDA MAUDE
Death Reports
Death reports associated with device
Incident Rate
Per 10,000 units in use
Recalls
No recalls on record
Estimated Units in Use
Based on market data estimates
Category Ranking
In Infusion Pumps by safety score
How This Compares
Other Infusion Pumps Devices
SERIES 3001 INTRA-AORTIC BALLOON PUMP
Unknown
SIGNATURE EDITION INFUSION PUMP
Unknown
PUMP MMT-512LNAL PRDGM INS CL EN US LN
Unknown
ART PILLOW 8MM PUMP SEGM UNIVE
Unknown
Important Context
Adverse event reports reflect reported incidents, not confirmed device failures. Higher numbers may indicate greater device usage, better reporting systems, or increased awareness. This data should be one factor in your research — always consult your physician.