Cytocell Ltd.: Medical Device Recall in 2019 - (Recall #: Z-1202-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Aquarius CSF1R/RPS14 (5q32-q33) Probe Red, Model LPH540-A Analyte specific reagent.

Product Classification:

Class III

Date Initiated: March 15, 2019

Date Posted: May 1, 2019

Recall Number: Z-1202-2019

Event ID: 82599

Reason for Recall:

There is an error in the chromomap included in the labeling for the product.

Status: Terminated

Product Quantity: 19

Code Information:

Lot numbers: 056996 061156 062616 062808

Distribution Pattern:

The products were distributed to the following US states: IL, TN.

Voluntary or Mandated:

Voluntary: Firm initiated