# FDA recall Z-2602-2017

> **Medtronic Inc.** · Class II · device recall initiated 2017-05-08.

## Product

MiniMed 620G Insulin Infusion Pump, Catalog No. MMT-1510, MMT-1710, MMT-1550, MMT-1750.

## Reason for recall

Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.

## Distribution

US and OUS    Angola  Aruba  Australia/NZ  Austria  Bahamas  Bahrain  Bangladesh  Belgium  Bolivia  Botswana  Bulgaria  Cayman Islands  Colombia  Costa Rica  Croatia  Cyprus  Czech Republic  Denmark  Dominican Republic  El Salvador  Estonia  Faroe Islands  Finland  France  Germany  Greece  Guadeloupe  Guatemala  Hong Kong  Hungary  Iceland  India  Iraq  Ireland  Israel  Italy  Japan  Jordan  Kazakhstan  Kenya  Korea  Kuwait  Latvia  Lebanon  Liechtenstein  Lithuania  Luxembourg  Macedonia  Malaysia  Martinique  Mauritius  Morocco  Namibia  Nepal  Netherlands  New Caledonia  Norway  Oman  Panama  Paraguay  Philippines  Poland  Portugal  Qatar  Reunion  Romania  San Marino  Saudi Arabia  Singapore  Slovakia  Slovenia  South Africa  Spain  Sweden  Switzerland  Tanzania  Thailand  Trinidad and Tobago  Turkey  United Arab Emirates  United Kingdom

## Key facts

- **Recall number:** Z-2602-2017
- **Recalling firm:** Medtronic Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-08
- **Report date:** 2017-06-28
- **Termination date:** 2021-01-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northridge, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2602-2017

## Citation

> AI Analytics. FDA recall Z-2602-2017. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/Z-2602-2017. Source: US FDA. Licensed CC0.

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