Cytocell Ltd.: Medical Device Recall in 2022 - (Recall #: Z-0814-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

TCL1 Breakapart Probe, Fluorescence in situ hybridisation (FISH) is a technique allows the visualisation of DNA sequences upon chromosome Catalog Number: LPH046-A

Product Classification:

Class III

Date Initiated: February 4, 2022

Date Posted: March 30, 2022

Recall Number: Z-0814-2022

Event ID: 89669

Reason for Recall:

May show unexpected locus specific signals in addition to those at 14q32.

Status: Terminated

Product Quantity: 1 unit

Code Information:

Lot 074612

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated