Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY, Item Number ART600; 2) A LINE TRAY, Item Number ART690
Summary
The FDA issued a Class I for Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY, Item Number ART600; by MEDLINE INDUSTRIES, LP - Northfield. Reason: The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub..
Details
Source
Device Recall
External ID
Z-0992-2025
Action Date
2025-02-05
Status
Ongoing
Category
device
Product Description
Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY, Item Number ART600; 2) A LINE TRAY, Item Number ART690
Lot/Code Info: 1) ART600 UDI-DI: 10653160312727 (each), 00653160312720 (case), Lot Number 2024110190; 2) ART690 UDI-DI: 10653160318019 (each), 00653160318012 (case), Lot Number 2024092490
Quantity Affected: 58 kits
Reason for Recall
The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.
Distribution
US Nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-12-31
Company
Northfield, IL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 158 device recalls issued in the same week, part of 413 device-related FDA actions this month.
MEDLINE INDUSTRIES, LP - Northfield has 822 FDA actions in our database, including 822 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (MEDLINE INDUSTRIES, LP - Northfield) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does MEDLINE INDUSTRIES, LP - Northfield have FDA actions?
MEDLINE INDUSTRIES, LP - Northfield has 822 FDA actions in our database, including 822 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0992-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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