FreshRecalls

Medline convenience kit: recall status

⚠ Recall found. Medline convenience kit is named in 6 official recalls in our current data. Details and the official notices are below — act on the remedy in the official notice.

Brand
Medline Industries

Recalls naming this model

FDA Class II · Medical device · June 24, 2026

Medline convenience kit recall — Medline Industries, LP

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

Official ID Z-2425-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kit recall — Medline Industries, LP

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

Official ID Z-2426-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kit recall — Medline Industries, LP

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

Official ID Z-2427-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kit recall — Medline Industries, LP

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

Official ID Z-2428-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kit recall — Medline Industries, LP

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

Official ID Z-2429-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kit recall — Medline Industries, LP

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

Official ID Z-2430-2026 · Official record ↗

See all Medline Industries recalls →

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Compiled from official public-domain CPSC, NHTSA, and FDA data. Sources last checked July 24, 2026 at 3:00 AM UTC.