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

Products covered by this recall
Model / numberProduct as published
ECVC8520PI CVC KIT 3L 7 FR 16 CM
CVI4880BNO CATH CENTRAL LINE KIT
ART35620G x 6" ARTERIAL CATHETER KIT
STCVC03MULTIMED 7FR, 16CM, 3L CVC BUNDLE
ARTNC217A-LINE KIT, NO CATH
ECVC1720PRESSURE INJ. CVC INSERTION BUNDLE
CVI4815DIALYSIS CATHETER INSERTION KIT
STCVC04MULTIMED 7FR, 20CM, 3L CVC BUNDLE
ECVC8520PI CVC KIT 3L 7 FR 16 CM
ART350ARTERIAL LINE TRAY
ECVC6355CVC INSERTION BUNDLE 8.5FR 4L 16CM
UVT980UMBILICAL VESSEL INSERTION TRAY
ECVC54807F, 16cm, 3L MAX BARRIER CVC BUNDLE
P972300AUCLA - FINE NEEDLE BIOPSY
ECVC825ATRIPLE LUMEN COMPLETE CATH KIT 16CM
ECVC86408.5F 4L 20CM CVC + BUNDLE
SPEC0291BULTRA CORE BIOPSY KIT
ECVC76053L 7FR 16CM CVC INSERTION BUNDLE
ECVC7330WATERBURY 3L CVC BUNDLE
ECVC76003L 7FR 20CM CVC INSERTION BUNDLE
Lot codes and dates

341 of 341 products

Products covered by this recall
#BarcodesProduct as published
11065316037719100653160377194Lot Number: 2026031790; 2) CVI4880B, UDI-DI: 10653160377191(each), 00653160377194(case)
21065316037537100653160375374Lot Number: 2026021190; 3) ART356, UDI-DI: 10653160375371(each), 00653160375374(case)
31065316036523500653160365238Lot Number: 2026011990; 4) STCVC03, UDI-DI: 10653160365235(each), 00653160365238(case)
41065316038335200653160383355Lot Number: 2026011990; 5) ARTNC217, UDI-DI: 10653160383352(each), 00653160383355(case)
51065316036576100653160365764Lot Number: 2025121190; 6) ECVC1720, UDI-DI: 10653160365761(each), 00653160365764(case)
61065316038604900653160386042Lot Number: 2025121990; 7) CVI4815, UDI-DI: 10653160386049(each), 00653160386042(case)
71065316033934200653160339345Lot Number: 2025121890; 8) STCVC04, UDI-DI: 10653160339342(each), 00653160339345(case)
81065316037510400653160375107Lot Number: 2025121890; 9) ECVC8520, UDI-DI: 10653160375104(each), 00653160375107(case)
91065316036205000653160362053Lot Number: 2025122290; 10) ART350, UDI-DI: 10653160362050(each), 00653160362053(case)
101065316033639600653160336399Lot Number: 2025120890; 11) ECVC6355, UDI-DI: 10653160336396(each), 00653160336399(case)
111065316037670500653160376708Lot Number: 2025120890; 12) UVT980, UDI-DI: 10653160376705(each), 00653160376708(case)
121065316038036800653160380361Lot Number: 2025120990; 13) ECVC5480, UDI-DI: 10653160380368(each), 00653160380361(case)
131065316037746700653160377460Lot Number: 2025122290; 14) P972300A, UDI-DI: 10653160377467(each), 00653160377460(case)
141065316038759600653160387599Lot Number: 2025120490; 15) ECVC825A, UDI-DI: 10653160387596(each), 00653160387599(case)
151065316039084800653160390841Lot Number: 2025120490; 16) ECVC8640, UDI-DI: 10653160390848(each), 00653160390841(case)
161065316038200300653160382006Lot Number: 2025122390; 17) SPEC0291B, UDI-DI: 10653160382003(each), 00653160382006(case)
171065316036449800653160364491Lot Number: 2026010790; 18) ECVC7605, UDI-DI: 10653160364498(each), 00653160364491(case)
181065316036456600653160364569Lot Number: 2026010890; 19) ECVC7330, UDI-DI: 10653160364566(each), 00653160364569(case)
191065316036444300653160364446Lot Number: 2026010790; 20) ECVC7600, UDI-DI: 10653160364443(each), 00653160364446(case)
201065316037720700653160377200Lot 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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Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Sep 19, 6:23 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.