# FDA recall Z-2542-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-05-21.

## Product

Medline Convenience Kits:  1) SUTURE TRAY, Model Number: SUT12260;   2) CHEST TUBE INSERTION TRAY, Model Number: MNS3390;   3) CONTRACEPTIVE IMPLANT INSERTION KIT, Model Number: MNS9715;   4) 20GX3" RADIAL ART LINE KIT, Model Number: ART351;   5) MYELOGRAM PACK, Model Number: P155615A;   6) CHEST TUBE INSERTION TRAY, Model Number: MNS3390;   7) LACERATION TRAY, Model Number: SUT18660A;   8) GENERAL BIOPSY TRAY, Model Number: MNS5985;   9) LACERATION TRAY, Model Number: DYNDL1351;   10) 20GX3" RADIAL ART LINE KIT, Model Number: ART351;   11) ARTERIAL LINE TRAY, Model Number: ART600;   12) SUTURE TRAY, Model Number: SUT12260;   13) ER SUTURING TRAY, Model Number: SUT9710C;   14) INCISION & DRAINAGE TRAY, Model Number: ID2060;   15) LACERATION TRAY - SNAG FREE, Model Number: SUT12265;   16) BIOPSY TRAY, Model Number: DYNDH1466;   17) GENERAL BIOPSY TRAY, Model Number: MNS5985;   18) SUTURE SET, Model Number: SUT19665;   19) MYELOGRAM-LF SAFE PACK, Model Number: P124863;   20) 20GX3" RADIAL ART LINE KIT, Model Number: ART351;   21) LACERATION TRAY, Model Number: SUT18660A;   22) 20GX6" FEMORAL ART LINE KIT, Model Number: ART352;   23) BIOPSY PACK, Model Number: DYNDH1699;   24) SUTURE TRAY, Model Number: SUT12260;   25) CHEST TUBE INSERTION TRAY, Model Number: MNS3390;   26) ARTHROGRAM TRAY, Model Number: SPEC0070B;   27) SUTURING SET, Model Number: SUT4155;   28) SUTURE TRAY, Model Number: SUT16080;   30) MYELOGRAM TRAY CHOICE, Model Number: DYNDH1213;   31) MYELOGRAM PACK, Model Number: P155615A;   32) LACERATION TRAY - SNAG FREE, Model Number: SUT12265

## Reason for recall

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.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2542-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-21
- **Report date:** 2026-07-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2542-2026

## Citation

> MORVS. FDA recall Z-2542-2026. Retrieved 2026-10-24 from https://api.morvs.ai/recall/Z-2542-2026. Source: US FDA. Licensed CC0.

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