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
| Model / number | Product as published |
|---|---|
ART1185B | ARTERIAL LINE INSERTION KIT |
ART255 | ARTERIAL LINE BUNDLE |
ART350 | ARTERIAL LINE TRAY |
ART355 | ARTERIAL LINE BUNDLE |
ART355 | ARTERIAL LINE BUNDLE |
ART475 | ARTERIAL LINE INSERTION TRAY |
ART535A | ARTERIAL LINE BUNDLE - OR |
ART545A | ARTERIAL LINE TRAY |
ART775C | ARTERIAL LINE INSERTION KIT |
ART840 | ARTERIAL LINE TRAY |
ART890B | ARTERIAL LINE KIT |
- Lot codes and dates
17 of 17 products
Products covered by this recall # Barcodes Product as published 1 1065316036759800653160367591Lot Number: 2024102590; 2) ART255 UDI-DI: 10653160367598(each), 00653160367591(case) 2 1065316036759800653160367591Lot Number: 2024082690; 3) ART255 UDI-DI: 10653160367598(each), 00653160367591(case) 3 1065316036205000653160362053Lot Number: 2024101590; 4) ART350 UDI-DI: 10653160362050(each), 00653160362053(case) 4 1065316036181700653160361810Lot Number: 2024093090; 5) ART355 UDI-DI: 10653160361817(each), 00653160361810(case) 5 1065316036181700653160361810Lot Number: 2024081290; 6) ART355 UDI-DI: 10653160361817(each), 00653160361810(case) 6 1065316036765900653160367652Lot Number: 2024112590; 7) ART475 UDI-DI: 10653160367659(each), 00653160367652(case) 7 1065316036765900653160367652Lot Number: 2024100790; 8) ART475 UDI-DI: 10653160367659(each), 00653160367652(case) 8 1065316036765900653160367652Lot Number: 2024073090; 9) ART475 UDI-DI: 10653160367659(each), 00653160367652(case) 9 1065316036765900653160367652Lot Number: 2024081590; 10) ART475 UDI-DI: 10653160367659(each), 00653160367652(case) 10 1065316036760400653160367607Lot Number: 2024090990; 11) ART535A UDI-DI: 10653160367604(each), 00653160367607(case) 11 1065316036760400653160367607Lot Number: 2024100890; 12) ART535A UDI-DI: 10653160367604(each), 00653160367607(case) 12 1065316037513500653160375138Lot Number: 2024080190; 13) ART545A UDI-DI: 10653160375135(each), 00653160375138(case) 13 1065316036610200653160366105Lot Number: 2024102890; 14) ART775C UDI-DI: 10653160366102(each), 00653160366105(case) 14 1065316036696600653160366969Lot Number: 2024083090; 15) ART840 UDI-DI: 10653160366966(each), 00653160366969(case) 15 1065316036696600653160366969Lot Number: 2024082390; 16) ART840 UDI-DI: 10653160366966(each), 00653160366969(case) 16 1065316036083400653160360837Lot Number: 2024093090; 17) ART890B UDI-DI: 10653160360834(each), 00653160360837(case) 17 Lot 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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