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Moderate recall: A hazard has been identified, with no injuries reported yet. Follow the steps below.

Diversatek Healthcare 2025-08-20 Health moderate FDA
Health · FDA · Recall #FDA-Z-2324-2025

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

Issued August 20, 2025 · Diversatek Healthcare

In August 2025, Diversatek Healthcare recalled the Zvu Anorectal Manometry Procedure Kit, REF: HRAM-PROC-10, a moderate health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

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.

What you should do

  1. 1 Stop using Zvu Anorectal Manometry Procedure Kit, REF: HRAM-PROC-10 right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Diversatek Healthcare to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Diversatek Healthcare
Category
Health
Recall date
August 20, 2025
Units affected
Not reported
Sold at
Worldwide - US Nationwide distribution in the states of NM, MA, CO, OH and the countries of Mongolia, South Korea.
Recall number
FDA-Z-2324-2025
Made in
United States
Issuing agency
FDA

In context

  • Diversatek Healthcare has 1 recall in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 691st Health recall we've logged in 2025.
Read the official FDA notice

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