Medtronic Inc. recalls MiniMed 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755.
- Recall date
- May 8, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2603-2017
- FDA classification
- Class II
- Brand / firm
- Medtronic Inc.
- Sold / distributed
- 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 Hungar…
Why it was recalled
Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
MiniMed 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755.
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