[Recalled] Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM — Coaxial cannula internal diameter and length of biopsy instruments exceed the e… | FDA 2023-04-11
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM |
|---|---|
| Brand / manufacturer | Bard Peripheral Vascular Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1564-2023 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 11 April 2023 |
| EAN / barcode | 00801741097089 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Coaxial cannula internal diameter and length of biopsy instruments exceed the external diameter and length of the biopsy needle, prohibiting the biopsy needle from properly fitting into the coaxial cannula and accessing the target tissue, which could lead to procedure delay, and insufficient sample acquisition requiring a repeat procedure.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Bard Peripheral Vascular Inc
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.