# FDA recall Z-1334-2026

> **Medline Industries, LP** · Class II · device recall initiated 2025-12-24.

## Product

Medline medical convenience kits packaged as:    ) LVAD DRESSING CHANGE TRAY, Kit SKU DM320C;   2) PORT AND IO ACCESS DRESSING KI, Kit SKU DT15780A;   3) PORT-A-CATH DRESSING CHANGE TR, Kit SKU DT16615;   4) LARGE BORE CENTRAL LINE DRSG C, Kit SKU DT19660;   5) CENTRAL LINE DRESSING CHANGE K, Kit SKU DT19665;   6) NEONATAL DRESSING CHANGE KIT, Kit SKU DT21495;   7) NICU CVC DRESSING CHANGE TRAY, Kit SKU DT22510A;   8) DRESSING CHANGE TRAY W/TEG CHG, Kit SKU DYNDC3114B;   9) DRESSING CHANGE KIT, Kit SKU DYNDC3351.

## Reason for recall

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1334-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-24
- **Report date:** 2026-02-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1334-2026

## Citation

> AI Analytics. FDA recall Z-1334-2026. Retrieved 2026-07-12 from https://api.ai-analytics.org/recall/Z-1334-2026. Source: US FDA. Licensed CC0.

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