BD Ready-to-Use Hydrophilic Catheter 14 Fr — Class II medical device recall Z-1061-2026
Ongoing recall by HANGZHOU BEVER MEDICAL DEVICES CO., LTD., reported 2026-01-21, distributed nationwide. Labeling error, Incorrect expiration date
| Recall number | Z-1061-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | HANGZHOU BEVER MEDICAL DEVICES CO., LTD., Hangzhou, China |
| Recall initiated | 2025-11-29 |
| Classified | 2026-01-12 |
| Reported by FDA | 2026-01-21 |
| Distributed | Nationwide (US) |
| Quantity | 149,310 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 06948796204063 |
| Lot numbers | T21823 |
| Model numbers | RTU14F |
Product
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1061-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.