FDAClass IIJanuary 24, 2024

6in Pressure Tubing recall

6IN PRESSURE TUBING, List Number MX20617

Why was 6in Pressure Tubing recalled?

There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication which may potentially lead to under infusion of medication.

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?

Lot Number: 4380614, 4416451

Product
6IN PRESSURE TUBING, List Number MX20617
Recalling firm
Smiths Medical Asd Inc
Quantity
31,685 total
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, UAE.
Recall date
January 24, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls