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FDAClass II · Medical device · Recalled June 24, 2026
Medline convenience kits recall — Medline Industries, LP
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Class II: may cause temporary or medically reversible health consequences.
View the official FDA enforcement record (openFDA) ↗
- Official recall ID
- Z-2434-2026
- Brand
- Medline Industries
- Classification
- Class II
- Units affected
- 49,654 kits total
- Recall status
- Ongoing
- Initiated
- Voluntary: Firm initiated
Description
Medline convenience kits: DAVINCI MAIN DYNJ908031D
Affected products
Companies & origin
- Recalling firm location
- Northfield, IL, United States
- Firm address
- 3 Lakes Dr, 60093-2753
Identifying details (verbatim from the notice)
- Product codes / lots
- DYNJ908031D UDI-DI 10198459632297 lot 26AMB067
- Distribution
- US Nationwide distribution. OUS distribution pending.
- Firm notified the public via
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- FDA event ID
- 98951
- Recall initiated
- April 27, 2026
- FDA classified
- June 12, 2026
- FDA report date
- June 24, 2026
Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim;
the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.
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