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CORPAK MedSystems recalls

CORPAK MedSystems has 3 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 31 May 2017. The most frequent reason is device malfunction.

Total recalls3since 2017

Last 12 months0reported

Class I00% of total

Ongoing0latest 31 May 2017

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why corpak medsystems is recalled

Device Malfunction3100%

Product types

Syringes & Needles3100%

By year

20173100%

All corpak medsystems recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
31 May 2017Device	CLASS II	Corflo, PEG Adaptor Repair Kit with ENFit Connectors, Size recalled	CORPAK MedSystems	Device Malfunction	CA, NH, VT
31 May 2017Device	CLASS II	Corflo, PEG Adaptor Repair Kit with ENFit Connectors, Size recalled	CORPAK MedSystems	Device Malfunction	CA, NH, VT
31 May 2017Device	CLASS II	Corflo PEG Kit, Pull recalled by CORPAK MedSystems	CORPAK MedSystems	Device Malfunction	CA, NH, VT

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.