Medical Action Industries, Inc. 306: Medical Device Recall in 2021 - (Recall #: Z-1559-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Kit: Blood Culture MAI Kit Part Number: 80076

Product Classification:

Class I

Date Initiated: April 9, 2021

Date Posted: May 19, 2021

Recall Number: Z-1559-2021

Event ID: 87722

Reason for Recall:

Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.

Status: Terminated

Product Quantity: 129 cases (20 kits per case)

Code Information:

Kit Number: 80076; UDI (GTIN): 20809160021269; Lot Number: 0000280292 (Expiration Date: 07/31/2021), 0000280766 (Expiration Date: 07/31/2021), 0000281206 (Expiration Date: 07/31/2021), 0000279153 (Expiration Date: 05/31/2021), and 0000280969 (Expiration Date: 06/30/2021)

Distribution Pattern:

Distributed US nationwide to OH, OR, FL and CA.

Voluntary or Mandated:

Voluntary: Firm initiated