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Medium risk Medical DevicesClass II

Medline Convenience Kits Recall

Medline Convenience Kits: 1) SUTURE TRAY, Model Number: SUT12260; 2) CHEST TUBE INSERTION TRAY, Model Number: MNS3390; 3) CONTRACEPTIVE IMPL

Updated May 21, 2026

Medline Convenience Kits containing Huons Lidocaine HCL Injection have been recalled due to quality issues found during an FDA inspection of the supplier's manufacturing site. The kits are used by healthcare providers for procedures like suturing, biopsies, and chest tube insertion.

Is the Medline Industries, LP recalled? Yes. This product was recalled by FDA on May 21, 2026. Details below.

What is recalled

Multiple Medline Convenience Kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules, including: Suture Tray (Model SUT12260), Chest Tube Insertion Tray (Model MNS3390), Contraceptive Implant Insertion Kit (Model MNS9715), 20G x 3" Radial Art Line Kit (Model ART351), Myelogram Pack (Model P155615A), Laceration Tray (Models SUT18660A, DYNDL1351, SUT12265), General Biopsy Tray (Model MNS5985), Arterial Line Tray (Model ART600), ER Suturing Tray (Model SUT9710C), Incision & Drainage Tray (Model ID2060), Biopsy Tray (Model DYNDH1466), Suture Set (Model SUT19665), Myelogram-LF Safe Pack (Model P124863), 20G x 6" Femoral Art Line Kit (Model ART352), Biopsy Pack (Model DYNDH1699), Arthrogram Tray (Model SPEC0070B), Suturing Set (Model SUT4155), Suture Tray (Model SUT16080), and Myelogram Tray Choice (Model DYNDH1213).

Am I affected

You are affected if you use or have received any of the Medline Convenience Kits listed above with the model numbers provided, especially those that contain the Huons Lidocaine HCL Injection 1% 10mg/ml 5mL ampules.

What to do right now

Stop using the recalled kits immediately. Contact Medline Industries or your healthcare facility procurement department to return the kits and obtain replacement units without the affected lidocaine ampules.

The hazard

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.

Brands affected

Medline Industries, LP
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-2542-2026
Classification
Class II
Recalled
May 21, 2026
Read the official notice

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