Medical Action Industries, Inc. 306

1 FDA enforcement actions

1 Total Recalls

0 Class I

1 Class II

0 Class III

Firm Details

Product Types: device
States: NC

All Recalls

Class II: Risk 06/11/2024 device

The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code. These blue foam pouches were misused due to misclassification of the GMDN.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.