FDAClass IIJanuary 21, 2026

BD Ready-to-Use Hydrophilic Catheter 14 Fr recall: Labeling Error

BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F

Why was BD Ready-to-Use Hydrophilic Catheter 14 Fr recalled?

Labeling error, Incorrect expiration date

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?

UDI: (01)06948796204063/Lot # T21823

Product
BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F
Recalling firm
HANGZHOU BEVER MEDICAL DEVICES CO., LTD.
Quantity
149310 units
Distribution
US Nationwide distribution in the state of GA.
Recall date
January 21, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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