Medline Surgery Tray (Medline) – Catheter Hub Defect (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medline General Surgery Tray Kits: 1) ARTERIAL LINE INSERTION KIT, Item Number ART1185B; 2) ARTERIAL LINE BUNDLE, Item Number ART255; 3) ARTERIAL LINE TRAY, Item Number ART350; 4) ARTERIAL LINE BUNDLE, Item Number ART355; 5) ARTERIAL LINE BUNDLE, Item Number ART355 ; 6) ARTERIAL LINE INSERTION TRAY, Item Number ART475; 7) ARTERIAL LINE BUNDLE - OR, Item Number ART535A; 8) ARTERIAL LINE TRAY, Item Number ART545A; 9) ARTERIAL LINE INSERTION KIT, Item Number ART775C; 10) ARTERIAL LINE TRAY, Item
Brand
MEDLINE INDUSTRIES, LP Northfield
Lot Codes / Batch Numbers
1) ART1185B UDI-DI: 10653160379225(each), 00653160379228(case), Lot Number: 2024102590, 2) ART255 UDI-DI: 10653160367598(each), 00653160367591(case), Lot Number: 2024082690, 3) ART255 UDI-DI: 10653160367598(each), 00653160367591(case), Lot Number: 2024101590, 4) ART350 UDI-DI: 10653160362050(each), 00653160362053(case), Lot Number: 2024093090, 5) ART355 UDI-DI: 10653160361817(each), 00653160361810(case), Lot Number: 2024081290, 6) ART355 UDI-DI: 10653160361817(each), 00653160361810(case), Lot Number: 2024112590, 7) ART475 UDI-DI: 10653160367659(each), 00653160367652(case), Lot Number: 2024100790, 8) ART475 UDI-DI: 10653160367659(each), 00653160367652(case), Lot Number: 2024073090, 9) ART475 UDI-DI: 10653160367659(each), 00653160367652(case), Lot Number: 2024081590, 10) ART475 UDI-DI: 10653160367659(each), 00653160367652(case), Lot Number: 2024090990, 11) ART535A UDI-DI: 10653160367604(each), 00653160367607(case), Lot Number: 2024100890, 12) ART535A UDI-DI: 10653160367604(each), 00653160367607(case), Lot Number: 2024080190, 13) ART545A UDI-DI: 10653160375135(each), 00653160375138(case), Lot Number: 2024102890, 14) ART775C UDI-DI: 10653160366102(each), 00653160366105(case), Lot Number: 2024083090, 15) ART840 UDI-DI: 10653160366966(each), 00653160366969(case), Lot Number: 2024082390, 16) ART840 UDI-DI: 10653160366966(each), 00653160366969(case), Lot Number: 2024093090, 17) ART890B UDI-DI: 10653160360834(each), 00653160360837(case), Lot Number: 2024100990
Products Sold
1) ART1185B UDI-DI: 10653160379225(each), 00653160379228(case), Lot Number: 2024102590; 2) ART255 UDI-DI: 10653160367598(each), 00653160367591(case), Lot Number: 2024082690; 3) ART255 UDI-DI: 10653160367598(each), 00653160367591(case), Lot Number: 2024101590; 4) ART350 UDI-DI: 10653160362050(each), 00653160362053(case), Lot Number: 2024093090; 5) ART355 UDI-DI: 10653160361817(each), 00653160361810(case), Lot Number: 2024081290; 6) ART355 UDI-DI: 10653160361817(each), 00653160361810(case), Lot Number: 2024112590; 7) ART475 UDI-DI: 10653160367659(each), 00653160367652(case), Lot Number: 2024100790; 8) ART475 UDI-DI: 10653160367659(each), 00653160367652(case), Lot Number: 2024073090; 9) ART475 UDI-DI: 10653160367659(each), 00653160367652(case), Lot Number: 2024081590; 10) ART475 UDI-DI: 10653160367659(each), 00653160367652(case), Lot Number: 2024090990; 11) ART535A UDI-DI: 10653160367604(each), 00653160367607(case), Lot Number: 2024100890; 12) ART535A UDI-DI: 10653160367604(each), 00653160367607(case), Lot Number: 2024080190; 13) ART545A UDI-DI: 10653160375135(each), 00653160375138(case), Lot Number: 2024102890; 14) ART775C UDI-DI: 10653160366102(each), 00653160366105(case), Lot Number: 2024083090; 15) ART840 UDI-DI: 10653160366966(each), 00653160366969(case), Lot Number: 2024082390; 16) ART840 UDI-DI: 10653160366966(each), 00653160366969(case), Lot Number: 2024093090; 17) ART890B UDI-DI: 10653160360834(each), 00653160360837(case), Lot Number: 2024100990;
MEDLINE INDUSTRIES, LP Northfield is recalling Medline General Surgery Tray Kits: 1) ARTERIAL LINE INSERTION KIT, Item Number ART1185B; 2) ARTERI due to The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.
Recommended Action
Per FDA guidance
A MEDICAL DEVICE RECALL notification letter dated 12/31/24 was sent to customers. REQUIRED ACTION: 1. Immediately check your stock for the affected item number and the affected lot numbers which can be located within the recall portal. Quarantine all affected product immediately. 2. Please use the link and the information below to complete your response form. Please list the quantity of affected product you have in inventory on the form. Even if you do not have any affected product in inventory, please complete and submit the response form. 3. Upon receipt of your submitted response form, your account will receive over-labels to place on affected inventory, with instructions for your staff to remove the affected component prior to using the kit. These labels will be provided via FedEx overnight, if applicable. The login for completing the response form is: Website link: https://recalls.medline.com Recall Reference #: R-24-278-FGX1 Recall Code: RECALL CODE 4. If you are a distributor, or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. If you have any questions, contact the Recall Department at 866-359-1704 or recalls@medline.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026