Medical Action Industries, Inc. 306: Medical Device Recall in 2021 - (Recall #: Z-1556-2021)

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: Midline Insertion DA. MAI Kit Part Number: 77981B

Product Classification:

Class I

Date Initiated: April 9, 2021

Date Posted: May 19, 2021

Recall Number: Z-1556-2021

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: 110 cases (5 kits per case)

Code Information:

Kit Number: 77981B; UDI (GTIN): 20809160284053; Lot Number: 0000281502 (Expiration Date: 04/08/2022), 0000282039 (Expiration Date: 04/08/2022), 0000274390 (Expiration Date: 07/09/2021), and 0000279101 (Expiration Date: 11/13/2021)

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated