The Recall Desk
ModerateFDA (Devices)·Z-2419-2026·Announced 2026-06-24

Medline central line dressing and port kits contain recalled Mastisol

Medline central line dressing kits, PICC/CVC/midline CHG dressing kits, port-a-cath kits and vein ablation packs are being recalled over a recalled lot of Mastisol Liquid Adhesive.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: FDA Class II recall where the described consequence is that a component becomes unusable rather than any patient hazard, which fits the Moderate band.

Plain-English summary

Medline convenience kits are being recalled, covering the Inpatient Central Line Dressing Kit (DYNDC3525), the PICC/CVC/Midline Dressing CHG Kit (DT13191A), the Port A Cath kit (CDS982047S) and the Vein Ablation Pack (DYNJ62889C). The action covers 49,654 kits in total across the connected Medline Mastisol recalls.

The stated reason is that the kits contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive. According to the notice, the butyrate tubing may crack during actuation and render the product unusable for application. The FDA classified the action as Class II. The source does not describe any patient hazard beyond the product being unusable.

Distribution was nationwide in the United States, with distribution outside the United States pending.

Facilities should identify affected stock using the kit numbers, UDI-DI codes and lot numbers in the recall notice and follow the instructions issued by Medline.

The recalled product

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
Affected units
49,654

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 34 recalled by Medline Industries, LP under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 34 products in this recall →