BARD MAGNUM Disposable Core Tissue Biopsy Needle REF: MN1410 MN 1420… — Class II medical device recall Z-3206-2024
Ongoing recall by Bard Peripheral Vascular Inc, reported 2024-10-02, distributed nationwide. Due to possible packaging damage (indentations/cuts) cause by manufacturing process. As a result of the packag
| Recall number | Z-3206-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bard Peripheral Vascular Inc, Tempe, AZ, United States |
| Recall initiated | 2024-08-02 |
| Classified | 2024-09-20 |
| Reported by FDA | 2024-10-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BR, CA, CL, CN, IN, JP, MX, MY, PE, PK |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00801741084249, 00801741084270, 00801741084287, 00801741084300, 00801741084355, 00801741084386 |
| Model numbers | 1420, MN1410, MN1410MN, MN1420, MN1610, MN1616, MN1820, MN2010 |
Product
BARD MAGNUM Disposable Core Tissue Biopsy Needle REF: MN1410 MN 1420 MN1610 MN1616 MN1820 MN2010 The Magnum Biopsy System (instrument and needles) is intended for use in obtaining biopsies from soft tissues such as liver, kidney, prostate, breast, spleen, lymph nodes and various soft tissue tumors.
Reason for recall
Due to possible packaging damage (indentations/cuts) cause by manufacturing process. As a result of the packaging damage, may cause the sterile barrier to be compromised.
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-3206-2024. 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.