# FDA recall Z-2419-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-04-27.

## Product

Medline convenience kits:    INPATIENT CENTRAL LN DRSG KIT  DYNDC3525    PICC/CVC/MIDLINE DRSG CHG KIT  DT13191A    PORT A CATH  CDS982047S    VEIN ABLATION PACK  DYNJ62889C

## Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

## Distribution

US Nationwide distribution. OUS distribution pending.

## Key facts

- **Recall number:** Z-2419-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-27
- **Report date:** 2026-06-24

- **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-2419-2026

## Citation

> MORVS. FDA recall Z-2419-2026. Retrieved 2026-10-17 from https://api.morvs.ai/recall/Z-2419-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*