---
title: "DeRoyal DEXMED ACCESS CENTER TRAY, containing Prevantics antiseptic (chlorhex... — FDA record Z-0880-2022 | Is It on Recall"
description: "A kit component, the PDI Prevantics Swab was recalled due to uncertain validation of test methods used to manufacture the products."
url: https://isitonrecall.com/recall/fda-device-z-0880-2022-deroyal-dexmed-access-center-tray-containing-prevantics-antiseptic-chlorhexidine-gluconate-and-isopr/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# DeRoyal DEXMED ACCESS CENTER TRAY, containing Prevantics antiseptic (chlorhexidine gluconate and isopropyl alcohol) s... — FDA record Z-0880-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 3, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: DeRoyal DEXMED ACCESS CENTER TRAY, containing Prevantics antiseptic (chlorhexidine gluconate and isopropyl alcohol) swab, for preparation of the patient skin prior to surgery or injection.
- **Reason**: A kit component, the PDI Prevantics Swab was recalled due to uncertain validation of test methods used to manufacture the products.
- **Classification**: Class II
- **Recalling firm**: DeRoyal Industries Inc
- **Quantity**: 1360 kits
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0880-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0880-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | SKU/Part Number 89-5300.07; UDI 00749756632317 Lot Numbers (Expiration Date): Lot 53059743 (exp 06/01/2022), Lot 53632941 (exp 06/01/2022), Lot 53666113 (exp 06/01/2022), Lot 54205909 (exp 06/01/2022), Lot 54279422 (exp 06/01/2022), Lot 54327332 (exp 06/01/2022), Lot 54473313 (exp 06/01/2022), Lot 55573404 (exp 06/01/2022) |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US distribution to Florida, New Jersey, and Tennessee

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Florida](https://isitonrecall.com/state/florida/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)

## Dates in the source

- **Report date**: Apr 13, 2022
- **Recall initiation date**: Mar 3, 2022
- **Center classification date**: Apr 6, 2022
- **Termination date**: Sep 15, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0880-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [DeRoyal Industries Inc records](https://isitonrecall.com/brand/deroyal-industries-inc/)