Quantimetrix Corporation: Medical Device Recall in 2018 - (Recall #: Z-2257-2018)

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:

Dropper Plus Point-of-Care Urinalysis Dipstick Control kit The Quantimetrix Dropper Plus Point-of-Care Urinalysis Dipstick Control is intended as a control for urinalysis reagent strips, microalbumin, and creatinine by the listed test methods, and as a control for confirmatory tests such as K-CHECK and Ictotest reagent tablets, and for hCG methods.

Product Classification:

Class III

Date Initiated: December 21, 2017

Date Posted: June 27, 2018

Recall Number: Z-2257-2018

Event ID: 80179

Reason for Recall:

The kits contained an incorrect lot of Dropper Plus Level 1 vials

Status: Terminated

Product Quantity: 20 kits

Code Information:

Lot 44450E

Distribution Pattern:

US Distribution to the state of : Kansas

Voluntary or Mandated:

Voluntary: Firm initiated