RecallRadar

FDA Device recall Z-2602-2017

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

On 2017-06-28 the FDA classified a Class II recall of MiniMed 620G Insulin Infusion Pump, Catalog No. MMT-1510, MMT-1710, MMT-1550, MMT-1750 by Medtronic, citing medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2602-2017
ClassificationClass II
Statusterminated
Initiated2017-05-08
Published2017-06-28
Last updated2026-09-13 11:54 UTC
CompanyMedtronic
Distributionn/a

Product

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

Reason

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

Identifiers

code_info
Serial Number (MMT-1510) NG1010153U NG1010155U NG1010156U NG1010157U NG1010158U NG1010159U NG1010160U NG1010163…Serial Number (MMT-1510) NG1010153U NG1010155U NG1010156U NG1010157U NG1010158U NG1010159U NG1010160U NG1010163U NG1010165U NG1010171U NG1010172U NG1010173U NG1010174U NG1010175U NG1010177U NG1010178U NG1010179U NG1010180U NG1010181U NG1010182U NG1010184U NG1010187U NG1010188U NG1010189U NG1010194U NG1010195U NG1010198U NG1010199U NG1010200U NG1010203U NG1010206U NG1010207U NG1010208U NG1010222U NG1010233U NG1010151U NG1010210U NG1010224U NG1010235U NG1010166U NG1010167U NG1010170U NG1010191U NG1010193U NG1010196U NG1010201U NG1010204U NG1010205U NG1010211U NG1010213U NG1010214U NG1010216U NG1010217U NG1010220U NG1010223U NG1010229U NG1010230U NG1010234U NG1010237U NG1010238U NG1010239U NG1010241U NG1010242U NG1010247U NG1010248U NG1010250U NG1010252U NG1010254U NG1010148U NG1010149U NG1010150U NG1010154U NG1010185U NG1010190U NG1010202U NG1010215U NG1010236U NG1010243U NG1010245U NG1010246U NG1010249U NG

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2602-2017%22

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