FDAClass IIApril 29, 2026

Medline Kits: 1) GENERAL LAPAROSCOPY recall

Medline Kits: 1) GENERAL LAPAROSCOPY, Model Number: CDS930027Y

Why was Medline Kits: 1) GENERAL LAPAROSCOPY recalled?

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

1) CDS930027Y, UDI-DI: 10198459303128(each), 40198459303129(case), Lot Number: 25EBE671

Product
Medline Kits: 1) GENERAL LAPAROSCOPY, Model Number: CDS930027Y
Recalling firm
Medline Industries, LP
Quantity
75 units
Distribution
US Nationwide distribution.
Recall date
April 29, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls