---
title: "Curad Quick Strip Fabric Bandages Containing 30 Bandages of 3/4\" x 3\", Medlin... — FDA record Z-0899-2026 | Is It on Recall"
description: "Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility"
url: https://isitonrecall.com/recall/fda-device-z-0899-2026-curad-quick-strip-fabric-bandages-containing-30-bandages-of-3-4-x-3-medline-item-number-cur1930p/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Curad Quick Strip Fabric Bandages Containing 30 Bandages of 3/4" x 3", Medline Item Number CUR1930P — FDA record Z-0899-2026

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 Oct 27, 2025. 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**: Curad Quick Strip Fabric Bandages Containing 30 Bandages of 3/4" x 3", Medline Item Number CUR1930P
- **Reason**: Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
- **Classification**: Class II
- **Recalling firm**: Medline Industries, LP
- **Quantity**: 18,000 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0899-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0899-2026%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 | UDI/DI 10888277702776 (each), 00888277702779 (box), 20888277702773 (case); ALL LOTS |

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

## Distribution

US, Guam, Canada, United Arab Emirates

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

## Dates in the source

- **Report date**: Dec 17, 2025
- **Recall initiation date**: Oct 27, 2025
- **Center classification date**: Dec 11, 2025

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-0899-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medline Industries, LP records](https://isitonrecall.com/brand/medline-industries-lp/)