Reported Feb 5, 2025 · Ongoing

Medline General Surgery Tray Kits

MEDLINE INDUSTRIES, LP - Northfield

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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 - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

Medline General Surgery Tray Kits

11 of 11 products

Products covered by this recall
Model / numberProduct as published
ART1185BARTERIAL LINE INSERTION KIT
ART255ARTERIAL LINE BUNDLE
ART350ARTERIAL LINE TRAY
ART355ARTERIAL LINE BUNDLE
ART355ARTERIAL LINE BUNDLE
ART475ARTERIAL LINE INSERTION TRAY
ART535AARTERIAL LINE BUNDLE - OR
ART545AARTERIAL LINE TRAY
ART775CARTERIAL LINE INSERTION KIT
ART840ARTERIAL LINE TRAY
ART890BARTERIAL LINE KIT
Lot codes and dates

17 of 17 products

Products covered by this recall
#BarcodesProduct as published
11065316036759800653160367591Lot Number: 2024102590; 2) ART255 UDI-DI: 10653160367598(each), 00653160367591(case)
21065316036759800653160367591Lot Number: 2024082690; 3) ART255 UDI-DI: 10653160367598(each), 00653160367591(case)
31065316036205000653160362053Lot Number: 2024101590; 4) ART350 UDI-DI: 10653160362050(each), 00653160362053(case)
41065316036181700653160361810Lot Number: 2024093090; 5) ART355 UDI-DI: 10653160361817(each), 00653160361810(case)
51065316036181700653160361810Lot Number: 2024081290; 6) ART355 UDI-DI: 10653160361817(each), 00653160361810(case)
61065316036765900653160367652Lot Number: 2024112590; 7) ART475 UDI-DI: 10653160367659(each), 00653160367652(case)
71065316036765900653160367652Lot Number: 2024100790; 8) ART475 UDI-DI: 10653160367659(each), 00653160367652(case)
81065316036765900653160367652Lot Number: 2024073090; 9) ART475 UDI-DI: 10653160367659(each), 00653160367652(case)
91065316036765900653160367652Lot Number: 2024081590; 10) ART475 UDI-DI: 10653160367659(each), 00653160367652(case)
101065316036760400653160367607Lot Number: 2024090990; 11) ART535A UDI-DI: 10653160367604(each), 00653160367607(case)
111065316036760400653160367607Lot Number: 2024100890; 12) ART535A UDI-DI: 10653160367604(each), 00653160367607(case)
121065316037513500653160375138Lot Number: 2024080190; 13) ART545A UDI-DI: 10653160375135(each), 00653160375138(case)
131065316036610200653160366105Lot Number: 2024102890; 14) ART775C UDI-DI: 10653160366102(each), 00653160366105(case)
141065316036696600653160366969Lot Number: 2024083090; 15) ART840 UDI-DI: 10653160366966(each), 00653160366969(case)
151065316036696600653160366969Lot Number: 2024082390; 16) ART840 UDI-DI: 10653160366966(each), 00653160366969(case)
161065316036083400653160360837Lot Number: 2024093090; 17) ART890B UDI-DI: 10653160360834(each), 00653160360837(case)
17Lot Number: 2024100990
Amount recalled
942 kits

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.

Using this product could cause serious injury, illness or death — stop using it now.

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.

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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, 6:19 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.