BioPince Full Core Biopsy Instrument 16ga x 15cm — Class II medical device recall Z-2427-2020
Terminated recall by Argon Medical Devices, Inc, reported 2020-07-01, distributed nationwide. Incorrect product labeling.
| Recall number | Z-2427-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Argon Medical Devices, Inc, Athens, TX, United States |
| Recall initiated | 2019-12-02 |
| Classified | 2020-06-25 |
| Reported by FDA | 2020-07-01 |
| Terminated | 2022-11-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, CA, ES |
| Reason classes | labeling |
| Lot numbers | 11277175 |
| Model numbers | 15CM, 16GA, 370-1580-01 |
Product
BioPince Full Core Biopsy Instrument 16ga x 15cm.,Use with Optional CO-Axial Needle MCXS1615BP. QTY.: 5/CS - Product Usage: The disposable, automatic BioPince Full Core Biopsy Instrument is used to obtain multiple core samples from soft tissue such as liver, kidney, abdominal masses, etc.
Reason for recall
Incorrect product labeling.
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-2427-2020. 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.