Diversatek Healthcare: Medical Device Recall in 2025 - (Recall #: Z-2324-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Zvu Anorectal Manometry Procedure Kit, REF: HRAM-PROC-10

Product Classification:

Class III

Date Initiated: June 4, 2025

Date Posted: August 20, 2025

Recall Number: Z-2324-2025

Event ID: 97282

Reason for Recall:

Anorectal manometry procedure kit outer kit label is mislabeled with an incorrect expiration date; the manufacturing date was used in place of the expiration date. All inner labels on kit components display the correct expiration date.

Status: Ongoing

Product Quantity: 8

Code Information:

UDI-DI: 00816734022863, Lot: 24752

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of NM, MA, CO, OH and the countries of Mongolia, South Korea.

Voluntary or Mandated:

Voluntary: Firm initiated