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
34 of 34 products
| Model / number | Product as published |
|---|---|
ECVC5995 | MULTIMED, 7FR, 20CM, 3L, CVC BUNDLE |
ECVC2625 | TRIPLE LUMEN CENTRAL LINE BUNDLE |
STCVC26US | INTROFLEX 6F, 1L, TB, US |
ECVC3720 | AVA HIGH FLOW |
3K16H1838 | CDP, MM, 3L, 7F, 16CM, H |
ECVC5610 | CVC Insertion Bundle 3L 7FR 20CM |
ECVC3810 | TRIPLE LUMEN CVC INSERTION BUNDLE |
ECVC2555 | 16CM TRIPLE LUMEN 7FR INSERT BUNDLE |
ECVC2750 | CENTRAL LINE BUNDLE W/7F, 20CM, 3L |
ECVC5200 | TRIPLE LUMEN COMPLETE CATH KIT |
ECVC7290 | TRIPLE LUMEN CVC 20CM BUNDLE W/O SUTURE |
ECVC3720 | AVA HIGH FLOW |
ECVC8215 | 7FR 3L 16CM CVC INSERTION BUNDLE |
ECVC2080 | CENTRAL LINE INSERTION BUNDLE |
ECVC8165 | 3L 7FR 16 CM CVC INSERTION TRAY |
ECVC6505 | VANTEX 7FR 3L 20CM CVC BUNDLE |
STCVC02 | VANTEX 7FR, 16CM, 3L CVC BUNDLE |
ECVC1377 | O.R. CVC TRIPLE LUMEN BUNDLE |
CMPI851LBA | INTROFLEX 8.5FR. 1L CVC BUNDLE |
STCVC49US | INTROFLEX 5F, 1L, TB, US, BAS |
- Lot codes and dates
34 of 34 products
Products covered by this recall # Barcodes Product as published 1 1065316033425500653160334258Lot Number: 2026011990; 2) ECVC2625, UDI-DI: 10653160334255(each), 00653160334258(case) 2 1065316034342400653160343427Lot Number: 2025121990; 3) STCVC26US, UDI-DI: 10653160343424(each), 00653160343427(case) 3 1065316034149900653160341492Lot Number: 2026010290; 4) ECVC3720, UDI-DI: 10653160341499(each), 00653160341492(case) 4 1065316034126000653160341263Lot Number: 2025123090; 5) 3K16H1838, UDI-DI: 10653160341260(each), 00653160341263(case) 5 1065316033504700653160335040Lot Number: 2025120590; 6) ECVC5610, UDI-DI: 10653160335047(each), 00653160335040(case) 6 1065316033601300653160336016Lot Number: 2025122290; 7) ECVC3810, UDI-DI: 10653160336013(each), 00653160336016(case) 7 1065316033657000653160336573Lot Number: 2025102390; 8) ECVC2555, UDI-DI: 10653160336570(each), 00653160336573(case) 8 1065316033421700653160334210Lot Number: 2025121190; 9) ECVC2750, UDI-DI: 10653160334217(each), 00653160334210(case) 9 1065316033615000653160336153Lot Number: 2025102490; 10) ECVC5200, UDI-DI: 10653160336150(each), 00653160336153(case) 10 1065316034493300653160344936Lot Number: 2025101490; 11) ECVC7290, UDI-DI: 10653160344933(each), 00653160344936(case) 11 1065316034149900653160341492Lot Number: 2025101490; 12) ECVC3720, UDI-DI: 10653160341499(each), 00653160341492(case) 12 1065316035899200653160358995Lot Number: 2025101690; 13) ECVC8215, UDI-DI: 10653160358992(each), 00653160358995(case) 13 1065316033440800653160334401Lot Number: 2025101790; 14) ECVC2080, UDI-DI: 10653160334408(each), 00653160334401(case) 14 1065316035874900653160358742Lot Number: 2025101690; 15) ECVC8165, UDI-DI: 10653160358749(each), 00653160358742(case) 15 1065316033632700653160336320Lot Number: 2025101390; 16) ECVC6505, UDI-DI: 10653160336327(each), 00653160336320(case) 16 1065316033682200653160336825Lot Number: 2025101490; 17) STCVC02, UDI-DI: 10653160336822(each), 00653160336825(case) 17 1065316033215200653160332155Lot Number: 2025101690; 18) ECVC1377, UDI-DI: 10653160332152(each), 00653160332155(case) 18 1065316034745300653160347456Lot Number: 2025101690; 19) CMPI851LBA, UDI-DI: 10653160347453(each), 00653160347456(case) 19 1065316034797200653160347975Lot Number: 2025090290; 20) STCVC49US, UDI-DI: 10653160347972(each), 00653160347975(case) 20 1065316035766700653160357660Lot Number: 2025092390; 21) ECVC8090, UDI-DI: 10653160357667(each), 00653160357660(case) - Amount recalled
- 967 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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