ClearanceBrief
Recall Z-1559-2021 ยท OFZ Blood Specimen Collection Kit (Excludes Hiv Testing)

Medical Action Industries, Inc. 306

Kit: Blood Culture MAI Kit Part Number: 80076

DateMay 12, 2021 (initiated Apr 9, 2021)
StatusTerminated
ReasonMedical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
Root causePackage design/selection
ActionA written notification letter titled, "URGENT: RECALL NOTIFICATION" was sent to all consignees on 04/09/2021 via email. The letter sent to the distributors instructs the consignees to immediately examine all inventory locations and discontinue use of Medical Action trays affected by this recall. The consignees are instructed to discard any inventory they may have on hand in accordance with the distributor's facility s standard procedures. If any of the affected products identified above were further distributed, the distributor is to ensure all end-users are appropriately notified of this p
Quantity129 cases (20 kits per case)
DistributionDistributed US nationwide to OH, OR, FL and CA.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.