Reported Jul 8, 2026 · Ongoing · Updated Sep 16, 2026
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
69 of 69 products
| Model / number | Product as published |
|---|---|
ECVC8520 | PI CVC KIT 3L 7 FR 16 CM |
CVI4880B | NO CATH CENTRAL LINE KIT |
ART356 | 20G x 6" ARTERIAL CATHETER KIT |
STCVC03 | MULTIMED 7FR, 16CM, 3L CVC BUNDLE |
ARTNC217 | A-LINE KIT, NO CATH |
ECVC1720 | PRESSURE INJ. CVC INSERTION BUNDLE |
CVI4815 | DIALYSIS CATHETER INSERTION KIT |
STCVC04 | MULTIMED 7FR, 20CM, 3L CVC BUNDLE |
ECVC8520 | PI CVC KIT 3L 7 FR 16 CM |
ART350 | ARTERIAL LINE TRAY |
ECVC6355 | CVC INSERTION BUNDLE 8.5FR 4L 16CM |
UVT980 | UMBILICAL VESSEL INSERTION TRAY |
ECVC5480 | 7F, 16cm, 3L MAX BARRIER CVC BUNDLE |
P972300A | UCLA - FINE NEEDLE BIOPSY |
ECVC825A | TRIPLE LUMEN COMPLETE CATH KIT 16CM |
ECVC8640 | 8.5F 4L 20CM CVC + BUNDLE |
SPEC0291B | ULTRA CORE BIOPSY KIT |
ECVC7605 | 3L 7FR 16CM CVC INSERTION BUNDLE |
ECVC7330 | WATERBURY 3L CVC BUNDLE |
ECVC7600 | 3L 7FR 20CM CVC INSERTION BUNDLE |
- Lot codes and dates
341 of 341 products
Products covered by this recall # Barcodes Product as published 1 1065316037719100653160377194Lot Number: 2026031790; 2) CVI4880B, UDI-DI: 10653160377191(each), 00653160377194(case) 2 1065316037537100653160375374Lot Number: 2026021190; 3) ART356, UDI-DI: 10653160375371(each), 00653160375374(case) 3 1065316036523500653160365238Lot Number: 2026011990; 4) STCVC03, UDI-DI: 10653160365235(each), 00653160365238(case) 4 1065316038335200653160383355Lot Number: 2026011990; 5) ARTNC217, UDI-DI: 10653160383352(each), 00653160383355(case) 5 1065316036576100653160365764Lot Number: 2025121190; 6) ECVC1720, UDI-DI: 10653160365761(each), 00653160365764(case) 6 1065316038604900653160386042Lot Number: 2025121990; 7) CVI4815, UDI-DI: 10653160386049(each), 00653160386042(case) 7 1065316033934200653160339345Lot Number: 2025121890; 8) STCVC04, UDI-DI: 10653160339342(each), 00653160339345(case) 8 1065316037510400653160375107Lot Number: 2025121890; 9) ECVC8520, UDI-DI: 10653160375104(each), 00653160375107(case) 9 1065316036205000653160362053Lot Number: 2025122290; 10) ART350, UDI-DI: 10653160362050(each), 00653160362053(case) 10 1065316033639600653160336399Lot Number: 2025120890; 11) ECVC6355, UDI-DI: 10653160336396(each), 00653160336399(case) 11 1065316037670500653160376708Lot Number: 2025120890; 12) UVT980, UDI-DI: 10653160376705(each), 00653160376708(case) 12 1065316038036800653160380361Lot Number: 2025120990; 13) ECVC5480, UDI-DI: 10653160380368(each), 00653160380361(case) 13 1065316037746700653160377460Lot Number: 2025122290; 14) P972300A, UDI-DI: 10653160377467(each), 00653160377460(case) 14 1065316038759600653160387599Lot Number: 2025120490; 15) ECVC825A, UDI-DI: 10653160387596(each), 00653160387599(case) 15 1065316039084800653160390841Lot Number: 2025120490; 16) ECVC8640, UDI-DI: 10653160390848(each), 00653160390841(case) 16 1065316038200300653160382006Lot Number: 2025122390; 17) SPEC0291B, UDI-DI: 10653160382003(each), 00653160382006(case) 17 1065316036449800653160364491Lot Number: 2026010790; 18) ECVC7605, UDI-DI: 10653160364498(each), 00653160364491(case) 18 1065316036456600653160364569Lot Number: 2026010890; 19) ECVC7330, UDI-DI: 10653160364566(each), 00653160364569(case) 19 1065316036444300653160364446Lot Number: 2026010790; 20) ECVC7600, UDI-DI: 10653160364443(each), 00653160364446(case) 20 1065316037720700653160377200Lot Number: 2026010790; 21) ECVC8110, UDI-DI: 10653160377207(each), 00653160377200(case) - Amount recalled
- 48075 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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