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Home › FDA recalls › BD Ready-to-Use Hydrophilic Catheter 14 Fr
CLASS II · ModerateFDA

HANGZHOU BEVER MEDICAL DEVICES CO., LTD. recalls BD Ready-to-Use Hydrophilic Catheter 14 Fr

📅 Nov 29, 2025 · 📍 Nationwide
Recalling company
HANGZHOU BEVER MEDICAL DEVICES CO., LTD.
Product
BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F
Reason
Labeling error, Incorrect expiration date
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
Nov 29, 2025
Reported
Jan 21, 2026
Distribution
US Nationwide distribution in the state of GA.
Status
Ongoing
Quantity
149310 units
Lot / codes
UDI: (01)06948796204063/Lot # T21823
Company location
Hangzhou
Recall type
Voluntary: Firm initiated
Recall number
Z-1061-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-1061-2026 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.