Centers For Disease Control and Prevention: Medical Device Recall in 2024 - (Recall #: Z-2220-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11

Product Classification:

Class II

Date Initiated: April 26, 2024

Date Posted: July 3, 2024

Recall Number: Z-2220-2024

Event ID: 94739

Reason for Recall:

The H5b component may fail to amplify, resulting in an inconclusive result.

Status: Terminated

Product Quantity: 191 units

Code Information:

Lot Code: Catalog # FluIVD03-11, lot 220307

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated