1 — Class II medical device recall Z-1574-2020
Terminated recall by Bard Peripheral Vascular Inc, reported 2020-04-01, distributed nationwide. Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant
| Recall number | Z-1574-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bard Peripheral Vascular Inc, Tempe, AZ, United States |
| Recall initiated | 2019-10-01 |
| Classified | 2020-03-26 |
| Reported by FDA | 2020-04-01 |
| Terminated | 2022-02-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | BR, CA, KR, MX, NZ |
| Quantity | 650 catheters |
| UPC / GTIN / UDI-DI | 00801741041570, 00801741041587 |
| Lot numbers | 7726954, RECQ1106, RECR2195, RECU1837 |
| Model numbers | 7726950, 7726954 |
Product
1. Groshong 9.5 Dual-Lumen CV Catheter, Ref: 7726950, UDI: (01)00801741041570; 2. Groshong 9.5 F Dual-Lumen CV Catheter, REF: 7726954, UDI: (01)00801741041587
Reason for recall
Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
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-1574-2020. 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.