Reported Jul 8, 2026 · Ongoing

Medline Convenience Kits

Medline Industries, LP

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

Medline Convenience Kits

31 of 31 products

Products covered by this recall
Model / numberProduct as published
SUT12260SUTURE TRAY
MNS3390CHEST TUBE INSERTION TRAY
MNS9715CONTRACEPTIVE IMPLANT INSERTION KIT
ART35120GX3" RADIAL ART LINE KIT
P155615AMYELOGRAM PACK
MNS3390CHEST TUBE INSERTION TRAY
SUT18660ALACERATION TRAY
MNS5985GENERAL BIOPSY TRAY
DYNDL1351LACERATION TRAY
ART35120GX3" RADIAL ART LINE KIT
ART600ARTERIAL LINE TRAY
SUT12260SUTURE TRAY
SUT9710CER SUTURING TRAY
ID2060INCISION & DRAINAGE TRAY
SUT12265LACERATION TRAY - SNAG FREE
DYNDH1466BIOPSY TRAY
MNS5985GENERAL BIOPSY TRAY
SUT19665SUTURE SET
P124863MYELOGRAM-LF SAFE PACK
ART35120GX3" RADIAL ART LINE KIT
Lot codes and dates

31 of 31 products

Products covered by this recall
#BarcodesProduct as published
10065316010043310653160100430Lot Number: 2026031190; 2) MNS3390, UDI-DI: 00653160100433(each), 10653160100430(case)
21065316029202900653160292022Lot Number: 2025120590; 3) MNS9715, UDI-DI: 10653160292029(each), 00653160292022(case)
31065316032375400653160323757Lot Number: 2025120890; 4) ART351, UDI-DI: 10653160323754(each), 00653160323757(case)
41088994221988940889942219880Lot Number: 2025120990; 5) P155615A, UDI-DI: 10889942219889(each), 40889942219880(case)
50065316010043310653160100430Lot Number: 2025120890; 6) MNS3390, UDI-DI: 00653160100433(each), 10653160100430(case)
61065316035930200653160359305Lot Number: 2025102790; 7) SUT18660A, UDI-DI: 10653160359302(each), 00653160359305(case)
70065316020440710653160204404Lot Number: 2025120890; 8) MNS5985, UDI-DI: 00653160204407(each), 10653160204404(case)
81088438927835240884389278353Lot Number: 2025120590; 9) DYNDL1351, UDI-DI: 10884389278352(each), 40884389278353(case)
91065316032375400653160323757Lot Number: 2025120190; 10) ART351, UDI-DI: 10653160323754(each), 00653160323757(case)
101065316031272700653160312720Lot Number: 2025112690; 11) ART600, UDI-DI: 10653160312727(each), 00653160312720(case)
110065316013094210653160130949Lot Number: 2025112690; 12) SUT12260, UDI-DI: 00653160130942(each), 10653160130949(case)
121065316033125400653160331257Lot Number: 2025112690; 13) SUT9710C, UDI-DI: 10653160331254(each), 00653160331257(case)
131065316031000600653160310009Lot Number: 2025103090; 14) ID2060, UDI-DI: 10653160310006(each), 00653160310009(case)
140065316013089810653160130895Lot Number: 2025101790; 15) SUT12265, UDI-DI: 00653160130898(each), 10653160130895(case)
151019348919375620193489193753Lot Number: 2025102390; 16) DYNDH1466, UDI-DI: 10193489193756(each), 20193489193753(case)
160065316020440710653160204404Lot Number: 2025102190; 17) MNS5985, UDI-DI: 00653160204407(each), 10653160204404(case)
171065316028857200653160288575Lot Number: 2025101690; 18) SUT19665, UDI-DI: 10653160288572(each), 00653160288575(case)
181088994214078740889942140788Lot Number: 2025102490; 19) P124863, UDI-DI: 10889942140787(each), 40889942140788(case)
191065316032375400653160323757Lot Number: 2025102090; 20) ART351, UDI-DI: 10653160323754(each), 00653160323757(case)
201065316035930200653160359305Lot Number: 2025101090; 21) SUT18660A, UDI-DI: 10653160359302(each), 00653160359305(case)
Amount recalled
15662 kits

This recall covers 24 products

The agency filed one notice per product. You are reading one of them; the other 23 are below.

11 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:01 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.