# FDA recall Z-1330-2026

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

## Product

1) UNIVERSAL KIT, Kit SKU DT22010B;   2) VAD ACCESS KIT, Kit SKU DT22790C;   3) VAD ACCESS KIT, Kit SKU DT22790C;   4) PROCEDURE TRAY, Kit SKU DYNDA2966A;   5) PROCEDURE TRAY, Kit SKU DYNDA2966A;   6) PEDIATRIC CENTRAL LINE SMALL, Kit SKU DYNDC2208C;   7) PORT DRESSING KIT, Kit SKU DYNDC3107;   8) NON STERILE DIALYSIS KIT, Kit SKU DYNDH1029C;   9) UMBILICAL TRAY W/3.5&5FR CATH, Kit SKU UVT1250;   10) UMBILICAL VESSEL TRAY, Kit SKU UVT835;   11) HEMODIALYSIS TRAY, Kit SKU VAR101HVAA.

## 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-1330-2026
- **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-1330-2026

## Citation

> AI Analytics. FDA recall Z-1330-2026. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-1330-2026. Source: US FDA. Licensed CC0.

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