QIAGEN: Medical Device Recall in 2018 - (Recall #: Z-2596-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

EZ1 DSP Virus Kit (48), IVD, REF 62724 intended for in vitro diagnostic use.

Product Classification:

Class II

Date Initiated: May 28, 2018

Date Posted: August 8, 2018

Recall Number: Z-2596-2018

Event ID: 80430

Reason for Recall:

Underfilled reagent well that could lead to incorrect results

Status: Terminated

Product Quantity: 287 pcs

Code Information:

UDI - 04053228000099 Lot - 160020069 Expiration - 11/01/19

Distribution Pattern:

Domestic - MD Internationally - AE, AU , CZ, DE, DZ, ES, FR, GB, HK , IE, IT, NO, RO & SA

Voluntary or Mandated:

Voluntary: Firm initiated