Class II — HANGZHOU BEVER MEDICAL DEVICES CO., LTD.
| Recalling firm | Hangzhou Bever Medical Devices Co., Ltd. |
|---|---|
| Registered facility | Hangzhou Bever Medical Devices Co., Ltd. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Labeling error, Incorrect expiration date |
| Product | BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F |
| Quantity | 149310 units |
| Distribution | US Nationwide distribution in the state of GA. |
| Initiated | 2025-11-29 |
| Classified | 2026-01-12 |
| Recall number | Z-1061-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — HANGZHOU BEVER MEDICAL DEVICES CO., LTD. (Z-1061-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98147/
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