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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Home Healthcare

BD Hydrophilic Catheter Recalled for Incorrect Expiration Date

Agency Publication Date: January 12, 2026
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Summary

HANGZHOU BEVER MEDICAL DEVICES CO., LTD. has recalled approximately 149,310 units of the BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female (REF: RTU14F). The recall was issued due to a labeling error where an incorrect expiration date was printed on the product. This issue affects units with Lot # T21823 and UDI (01)06948796204063.

Risk

An incorrect expiration date may lead to the use of a catheter that has exceeded its validated shelf life. This could potentially compromise the device's sterility or physical performance, which may increase the risk of infection or injury to the patient.

What You Should Do

  1. This recall involves the BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female (REF: RTU14F) identified by Lot # T21823 and UDI (01)06948796204063.
  2. Stop using the recalled device immediately.
  3. Contact the manufacturer, HANGZHOU BEVER MEDICAL DEVICES CO., LTD., or your medical distributor to arrange for the return, replacement, or correction of the affected catheters.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for any additional questions regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female
Variants: 14 Fr (4.7 mm), Straight Tip, Coated, Female
Model / REF:
RTU14F
Lot Numbers:
T21823
UDI:
(01)06948796204063

Quantity affected: 149,310 units. Recall Number: Z-1061-2026.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98147
Status: Active
Manufacturer: HANGZHOU BEVER MEDICAL DEVICES CO., LTD.
Sold By: Medical supply distributors
Manufactured In: China
Units Affected: 149310 units
Distributed To: Georgia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.