FDA Recall Database: Class I Recall: Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL… by Medline Industries, LP

Key facts

What this classification means

A Class I recall is FDA's most serious classification. FDA assigns Class I when there is a reasonable probability that use of, or exposure to, the recalled product will cause serious adverse health consequences or death. This classification does not mean harm has already occurred in every case — it reflects FDA's assessment of the realistic worst-case risk profile of the defect described in the recall, based on the reason for recall reported by the firm. Class I recalls receive the closest FDA monitoring of the three classes: the recalling firm typically must submit a recall strategy, periodic status reports, and effectiveness checks confirming that the affected lots have actually been removed from distribution or corrected in the field. FDA's Center for Devices and Radiological Health (for devices) or Center for Drug Evaluation and Research (for drugs) reviews the classification and can require additional corrective action if the initial response is judged insufficient. Because Class I is reserved for the highest-risk defects, professionals and consumers handling an affected lot are generally advised to treat the recall as time-sensitive rather than routine.

What consumers should do

Facilities and clinicians holding an affected lot or unit should stop using it for the indication described in the recall notice and quarantine remaining stock pending instructions from Medline Industries, LP. FDA recall records for devices typically direct the recalling firm to notify known accounts (hospitals, distributors, clinics) directly with a recall letter describing the specific corrective action — replacement, field correction, or return. Anyone who received Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE, Model Number: ACC010890; 2) OPEN HEART A OVERHEAD, Model Number: DYNJ910066; 3) OPEN HEART, Model Number: DYNJ9855016V; 4) OPEN HEART, Model Number: DYNJ9855016X through a distributor rather than directly from Medline Industries, LP should still confirm with their supplier whether their specific lot or serial number is on the affected list, since recall notices are lot- or unit-specific and not every unit of a product line is necessarily included. Questions about a specific unit's status should go to Medline Industries, LP directly or to the distributor that supplied it; Argus HQ is a public-record aggregator, not the recalling firm, and cannot confirm individual unit status.

Medline Industries, LP’s FDA history

Argus HQ has recorded 242 total FDA actions tied to Medline Industries, LP: 0 warning letters, 242 recalls, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

Is Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE, Model Number: ACC01 recalled?

Yes. FDA lists a Class I recall by Medline Industries, LP for Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE, Model Number: ACC010890; 2) OPEN HEART A OVERHEAD, Model Number: DYNJ910066; 3) OPEN HEART, Model Number: DYNJ9855016V; 4) OPEN HEART, Model Number: DYNJ9855016X, reported July 1, 2026, with status "Ongoing." FDA recall number: Z-2455-2026.

What is the recall class for Medline Industries, LP's Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE, recall?

FDA classified this recall as Class I. Class I is FDA's most serious classification, reserved for defects with a reasonable probability of serious health consequences or death.

Why was Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE, recalled?

FDA's recall record states the reason as: 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 d

Who should I contact about this recall?

Contact Medline Industries, LP directly, or the distributor/pharmacy that supplied the product, to confirm whether your specific lot or unit is affected. Argus HQ aggregates the public FDA recall record and is not the recalling firm.

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