Bard Marquee Disposable Core Biopsy Instrument Kit — Class II medical device recall Z-0027-2024
Ongoing recall by Bard Peripheral Vascular Inc, reported 2023-10-11, distributed nationwide. Diameter mismatch between coaxial and biopsy needle (cutting cannula) in disposable core biopsy instrument kit
| Recall number | Z-0027-2024 |
|---|---|
| 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 | 2023-08-10 |
| Classified | 2023-10-04 |
| Reported by FDA | 2023-10-11 |
| Distributed | Nationwide (US) |
| Quantity | 1,545 |
| UPC / GTIN / UDI-DI | 00801741097393 |
| Lot numbers | 0001480774 |
| Model numbers | MQK2016 |
| Expiration dates | 2025-07-28 |
Product
Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
Reason for recall
Diameter mismatch between coaxial and biopsy needle (cutting cannula) in disposable core biopsy instrument kits, where the coaxial cannula inner diameter prohibits the biopsy needle (cutting cannula) from properly fitting into the coaxial cannula and accessing target tissue, which may lead to repeated procedure, and procedural complications, such as pain/discomfort, pneumothorax, and bleeding.
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-0027-2024. 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.