Z-1061-2026 Class II Ongoing
FDA device recall Z-1061-2026 was initiated by HANGZHOU BEVER MEDICAL DEVICES CO., LTD. on November 29, 2025 and is designated Class II. Reason for recall: Labeling error, Incorrect expiration date The recall status is ongoing. Affected quantity: 149310 units.
Recall Details
- Product Type
- Devices
- Report Date
- January 21, 2026
- Initiation Date
- November 29, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 149310 units
Product Description
BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F
Reason for Recall
Labeling error, Incorrect expiration date
Distribution Pattern
US Nationwide distribution in the state of GA.
Code Information
UDI: (01)06948796204063/Lot # T21823