FDA recall Z-2605-2017

Product

MiniMed 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760.

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

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

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2605-2017