Diversatek Healthcare recalls Zvu Anorectal Manometry Procedure Kit REF HRAM-PROC-10 due to mislabeled expiration date on outer kit. All inner labels show correct dates. No immediate safety risk but affects medical use.
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.
Diversatek Healthcare is recalling their Zvu Anorectal Manometry Procedure Kit (REF: HRAM-PROC-10) because the outer kit label has an incorrect expiration date. This could lead to using expired medical supplies, which might affect test accuracy or patient safety. The inner labels on components show the correct expiration dates.
The outer kit label shows the manufacturing date instead of the expiration date. This means the kit may be used after its actual expiration date, potentially leading to inaccurate test results or compromised patient care. Inner labels on components correctly show expiration dates.
Healthcare providers using the Zvu Anorectal Manometry Procedure Kit for medical testing. Patients receiving these tests may be at risk if the expired supplies cause inaccurate results.
Check for the product name 'Zvu Anorectal Manometry Procedure Kit' with reference number HRAM-PROC-10. Look for the UDI-DI code 00816734022863 and lot number 24752 on the outer kit.
Verify the expiration date on the outer kit label matches the inner labels of components. If the outer label shows a manufacturing date instead of expiration, it is recalled.
No immediate safety risk. The hazard is a mislabeled expiration date on the outer kit, which could affect test accuracy but does not cause injury or illness.
Look for the product name 'Zvu Anorectal Manometry Procedure Kit' with reference number HRAM-PROC-10, UDI-DI code 00816734022863, and lot number 24752 on the outer kit.
The recall record does not specify a return or remedy, so no action is required beyond checking the label dates.
We’ve drafted a message you can send Diversate: Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2324-2025 — Diversate: Healthcare Diversate: Healthcare Hello, I own a Diversate: Healthcare that is covered by recall Z-2324-2025 from Diversate: Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
