Data Foundry

Medical device recalls 2026

Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE — Class I medical device recall Z-2455-2026

Ongoing recall by Medline Industries, LP, reported 2026-07-01, distributed nationwide. The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP a

Recall numberZ-2455-2026
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedline Industries, LP, Northfield, IL, United States
Recall initiated2026-05-06
Classified2026-06-24
Reported by FDA2026-07-01
DistributedNationwide (US)
Quantity503 units
UPC / GTIN / UDI-DI10195327565596, 10198459019951, 10198459139833, 10198459571374, 40195327565597, 40198459019952, 40198459139834, 40198459571375
Lot numbers24FDB427, 25ABH622, 25ADB324, 25BDA811, 25CBA788, 25CBF665, 25DBR616, 25DDB415, 25DDC095, 25FBA415, 25FDB473, 25GDA336, 25HBT666, 25KBO109
Model numbersACC010890, DYNJ910066, DYNJ9855016V, DYNJ9855016X

Product

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

Reason for recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2455-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.