---
title: "Dover\" 100% SILICONE FOLEY TRAY, NEEDLELESS, 14 FR (4.7 MM), 5 CC, 2000 ML DR... — FDA record Z-1052-2024 | Is It on Recall"
description: "Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist."
url: https://isitonrecall.com/recall/fda-device-z-1052-2024-dover-100-silicone-foley-tray-needleless-14-fr-4-7-mm-5-cc-2000-ml-drain-bag-drain-spout-dover-hydro/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Dover" 100% SILICONE FOLEY TRAY, NEEDLELESS, 14 FR (4.7 MM), 5 CC, 2000 ML DRAIN BAG, DRAIN SPOUT; Dover" HYDROGEL CO... — FDA record Z-1052-2024

Reported ongoing

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 Dec 4, 2023. 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**: Dover" 100% SILICONE FOLEY TRAY, NEEDLELESS, 14 FR (4.7 MM), 5 CC, 2000 ML DRAIN BAG, DRAIN SPOUT; Dover" HYDROGEL COATED LATEX FOLEY CATHETER KIT, 5 CC, 2-WAY, 14 FR (4.7 MM), 10 CC WATER SYRINGE
- **Reason**: Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.
- **Classification**: Class I
- **Recalling firm**: Cardinal Health 200, LLC
- **Quantity**: 924 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1052-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1052-2024%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 | 1814, UDI/DI 20884521003528 (cs), 10884521003521 (ea), Lot Numbers: 22210206164, 2211627364, 2231919964 |

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

## Distribution

US and EMEA, Japan, Latin America

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Feb 28, 2024
- **Recall initiation date**: Dec 4, 2023
- **Center classification date**: Feb 16, 2024

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-1052-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Cardinal Health 200, LLC records](https://isitonrecall.com/brand/cardinal-health-200-llc/)