The Recall Desk
ModerateFDA (Devices)·Z-2434-2026·Announced 2026-06-24

Medline da Vinci main kits contain recalled Mastisol liquid adhesive

Medline da Vinci Main convenience kits are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.

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

The Medline da Vinci Main convenience kit, SKU DYNJ908031D, is being recalled. 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.

Affected product is UDI-DI 10198459632297, lot 26AMB067. Distribution was nationwide in the United States, with distribution outside the United States pending.

Facilities should identify affected stock using the kit number, UDI-DI and lot number above and follow the instructions issued by Medline.

The recalled product

Product
Medline convenience kits: DAVINCI MAIN DYNJ908031D
Affected units
49,654

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • DYNJ908031D UDI-DI 10198459632297 lot 26AMB067

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 →