CORPAK MedSystems, Inc. Recalls

Overview of recall records associated with CORPAK MedSystems, Inc., including dates, categories and classifications where available.

3recall records

May 31, 2017latest record date

May 31, 2017earliest record date

Recall history in this database

Classification mix: Class II: 3.

Medical DeviceMay 31, 2017

CORPAK MedSystems CORFLO PEG Kit, Pull 16FR recall — FDA Z-2163-2017

Firm is initiating voluntary correction of CORFLO PEG with ENFit. Barb connector (stem) of the adapter may break unexpectedly when exposed to stress.

Class IIFDA: TerminatedCORPAK MedSystems, Inc.

Medical DeviceMay 31, 2017

CORPAK MedSystems CORFLO, PEG Adaptor Repair Kit with ENFit Connectors, Size: 12FR (4mm) recall — FDA Z-2161-2017

Firm is initiating voluntary correction of CORFLO PEG with ENFit. Barb connector (stem) of the adapter may break unexpectedly when exposed to stress.

Class IIFDA: TerminatedCORPAK MedSystems, Inc.

Medical DeviceMay 31, 2017

CORPAK MedSystems CORFLO, PEG Adaptor Repair Kit with ENFit Connectors, Size: 16FR recall — FDA Z-2162-2017

Firm is initiating voluntary correction of CORFLO PEG with ENFit. Barb connector (stem) of the adapter may break unexpectedly when exposed to stress.

Class IIFDA: TerminatedCORPAK MedSystems, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies CORPAK MedSystems, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.