FDA recall, , Moderate risk
HANGZHOU BEVER MEDICAL DEVICES BD Ready-to-Use Hydrophilic Catheter
The BD Ready-to-Use Hydrophilic Catheter has a labeling error with an incorrect expiration date.
Summary by Recall Canary from the FDA notice
What happened
HANGZHOU BEVER MEDICAL DEVICES CO., LTD., located in Hangzhou, China, began the recall of the BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female on November 29, 2025, due to a labeling error with an incorrect expiration date. The recall involves 149310 units distributed in the state of Georgia.
The FDA added the recall to its Enforcement Report on January 12, 2026, and classified it on January 12, 2026. The FDA's weekly enforcement report on January 21, 2026 included the recall.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the UDI-DI and lot code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F
- UDI-DI
- 06948796204063
- Lot code
- T21823
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the state of Georgia.
- Company
- HANGZHOU BEVER MEDICAL DEVICES CO., LTD.Hangzhou, China
- Hazard
- Labeling error
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98147
- Recall number
- Z-1061-2026
- Quantity recalled
- 149310 units
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
