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MEDLINE ART890BRecalls & reported problems

Medline Industries, Inc. · ARTERIAL LINE KIT · Class 2

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. May 21, 2026Open, Classified

    The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

    Z-2543-2026 · Root cause: Nonconforming Material/Component · FDA record ↗

  2. Dec 31, 2024Open, Classified

    The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.

    Z-0991-2025 · Root cause: Process design · FDA record ↗

Other I.V. start kit devices

All I.V. start kit devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.