FDAClass I · Medical device · Recalled July 1, 2026

Medline Convenience Kits recall — Medline Industries, LP

Hazard: The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.

Class I: most serious — reasonable probability of serious health consequences or death.

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2454-2026
Brand: Medline Industries
Classification: Class I
Units affected: 233 units
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Description

Medline Convenience Kits: 1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC011142; 2) CENTRAL AND ARTERIAL LINE TOTE, Model Number: DYNJ8407

Affected products

Medline Convenience Kits

Companies & origin

Recalling firm location: Northfield, IL, United States
Firm address: 3 Lakes Dr, N/A, 60093-2753

Identifying details (verbatim from the notice)

Product codes / lots: 1) ACC011142, UDI-DI: 10198459721342(each), 40198459721343(case), Lot Number: 26DDA462; 2) ACC011142, UDI-DI: 10198459721342(each), 40198459721343(case), Lot Number: 26DDA547; 3) DYNJ8407, UDI-DI: 10198459704543(each), 40198459704544(case), Lot Number: 26DBB599
Distribution: US Nationwide.
Firm notified the public via: Letter
FDA event ID: 99043
Recall initiated: May 6, 2026
FDA classified: June 24, 2026
FDA report date: July 1, 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 24, 2026 at 12:00 AM UTC.

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