Bard Mission Disposable Core Biopsy Instrument Kit — Class II medical device recall Z-0643-2024
Ongoing recall by Bard Peripheral Vascular Inc, reported 2024-01-17, distributed nationwide. The internal diameter of the coaxial cannula may be smaller or larger than the external diameter of the biopsy
| Recall number | Z-0643-2024 |
|---|---|
| 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 | 2023-11-08 |
| Classified | 2024-01-05 |
| Reported by FDA | 2024-01-17 |
| Distributed | Nationwide (US) |
| Quantity | 1,243,937 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00801741097058, 00801741097065, 00801741097072, 00801741097089, 00801741097096, 00801741097102, 00801741142543, 00801741142550, 00801741142567, 00801741142574, 00801741142581 |
| Lot numbers | 1410MSK, 1416MSK, 1610MSK, 1616MSK, 1810MSK, 1816MSK/00801741097065, 1820MSK, 1825MSK, 2010MSK/00801741097089, 2016MSK, 2020MSK |
Product
Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit 14G x 16CM; 1610MSK/ Mission Kit 16G x 10CM; 1616MSK/ Mission Kit 16G x 16CM; 1810MSK/ Mission Kit 18G x 10CM; 1816MSK/ Mission Kit 18G x 16CM; 1820MSK/ Mission Kit 18G x 20CM; 1825MSK/ Mission Kit 18G x 25CM; 2010MSK/ Mission Kit 20G x 10CM; 2016MSK/ Mission Kit 20G x 16CM; 2020MSK/ Mission Kit 20G x 20CM
Reason for recall
The internal diameter of the coaxial cannula may be smaller or larger than the external diameter of the biopsy needle, and the length of the cannula may exceed the stated length on the label. As a result, the biopsy needle may not fit properly into the coaxial cannula, preventing access to the target tissue, which could lead to tissue injury, longer and repeat procedures.
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-0643-2024. 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.