← FDA ENFORCEMENT
Z-1061-2026Class II
HANGZHOU BEVER MEDICAL DEVICES CO., LTD.
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
HANGZHOU BEVER MEDICAL DEVICES CO., LTD.
Product type
Device
Status
Ongoing
Report date
2026-01-21
Distribution
US Nationwide distribution in the state of GA.
Product quantity
149310 units
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Validation & QualificationReason for recall
Labeling error, Incorrect expiration date
Product description
BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F
Code / lot info
UDI: (01)06948796204063/Lot # T21823
Other recalls SPEQ maps to Validation & Qualification
2026-10-21Class IIZydus Pharmaceuticals (USA) Inc2026-10-21Class IIIMagellan Diagnostics, Inc.2026-10-21Class IIMicrogenics Corporation2026-10-14Class IICipla USA, Inc.
See all Validation & Qualification recalls →Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →