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
| Model / number | Product as published |
|---|---|
SUT12260 | SUTURE TRAY |
MNS3390 | CHEST TUBE INSERTION TRAY |
MNS9715 | CONTRACEPTIVE IMPLANT INSERTION KIT |
ART351 | 20GX3" RADIAL ART LINE KIT |
P155615A | MYELOGRAM PACK |
MNS3390 | CHEST TUBE INSERTION TRAY |
SUT18660A | LACERATION TRAY |
MNS5985 | GENERAL BIOPSY TRAY |
DYNDL1351 | LACERATION TRAY |
ART351 | 20GX3" RADIAL ART LINE KIT |
ART600 | ARTERIAL LINE TRAY |
SUT12260 | SUTURE TRAY |
SUT9710C | ER SUTURING TRAY |
ID2060 | INCISION & DRAINAGE TRAY |
SUT12265 | LACERATION TRAY - SNAG FREE |
DYNDH1466 | BIOPSY TRAY |
MNS5985 | GENERAL BIOPSY TRAY |
SUT19665 | SUTURE SET |
P124863 | MYELOGRAM-LF SAFE PACK |
ART351 | 20GX3" RADIAL ART LINE KIT |
- Lot codes and dates
31 of 31 products
Products covered by this recall # Barcodes Product as published 1 0065316010043310653160100430Lot Number: 2026031190; 2) MNS3390, UDI-DI: 00653160100433(each), 10653160100430(case) 2 1065316029202900653160292022Lot Number: 2025120590; 3) MNS9715, UDI-DI: 10653160292029(each), 00653160292022(case) 3 1065316032375400653160323757Lot Number: 2025120890; 4) ART351, UDI-DI: 10653160323754(each), 00653160323757(case) 4 1088994221988940889942219880Lot Number: 2025120990; 5) P155615A, UDI-DI: 10889942219889(each), 40889942219880(case) 5 0065316010043310653160100430Lot Number: 2025120890; 6) MNS3390, UDI-DI: 00653160100433(each), 10653160100430(case) 6 1065316035930200653160359305Lot Number: 2025102790; 7) SUT18660A, UDI-DI: 10653160359302(each), 00653160359305(case) 7 0065316020440710653160204404Lot Number: 2025120890; 8) MNS5985, UDI-DI: 00653160204407(each), 10653160204404(case) 8 1088438927835240884389278353Lot Number: 2025120590; 9) DYNDL1351, UDI-DI: 10884389278352(each), 40884389278353(case) 9 1065316032375400653160323757Lot Number: 2025120190; 10) ART351, UDI-DI: 10653160323754(each), 00653160323757(case) 10 1065316031272700653160312720Lot Number: 2025112690; 11) ART600, UDI-DI: 10653160312727(each), 00653160312720(case) 11 0065316013094210653160130949Lot Number: 2025112690; 12) SUT12260, UDI-DI: 00653160130942(each), 10653160130949(case) 12 1065316033125400653160331257Lot Number: 2025112690; 13) SUT9710C, UDI-DI: 10653160331254(each), 00653160331257(case) 13 1065316031000600653160310009Lot Number: 2025103090; 14) ID2060, UDI-DI: 10653160310006(each), 00653160310009(case) 14 0065316013089810653160130895Lot Number: 2025101790; 15) SUT12265, UDI-DI: 00653160130898(each), 10653160130895(case) 15 1019348919375620193489193753Lot Number: 2025102390; 16) DYNDH1466, UDI-DI: 10193489193756(each), 20193489193753(case) 16 0065316020440710653160204404Lot Number: 2025102190; 17) MNS5985, UDI-DI: 00653160204407(each), 10653160204404(case) 17 1065316028857200653160288575Lot Number: 2025101690; 18) SUT19665, UDI-DI: 10653160288572(each), 00653160288575(case) 18 1088994214078740889942140788Lot Number: 2025102490; 19) P124863, UDI-DI: 10889942140787(each), 40889942140788(case) 19 1065316032375400653160323757Lot Number: 2025102090; 20) ART351, UDI-DI: 10653160323754(each), 00653160323757(case) 20 1065316035930200653160359305Lot 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.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Medline Industries, LP recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.