---
title: "BX2 Needle Guide, Part Number 644-094, tool for performing needle-guided (or ... — FDA record Z-1892-2025 | Is It on Recall"
description: "During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle guide can cause a pinhole breach in the transducer cov"
url: https://isitonrecall.com/recall/fda-device-z-1892-2025-bx2-needle-guide-part-number-644-094-tool-for-performing-needle-guided-or-catheter-procedures-with-t/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# BX2 Needle Guide, Part Number 644-094, tool for performing needle-guided (or catheter) procedures with the use of dia... — FDA record Z-1892-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 1, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: BX2 Needle Guide, Part Number 644-094, tool for performing needle-guided (or catheter) procedures with the use of diagnostic ultrasound transducers
- **Reason**: During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle guide can cause a pinhole breach in the transducer cover when latching the guide in place.
- **Classification**: Class II
- **Recalling firm**: Civco Medical Instruments Co. Inc.
- **Quantity**: 506 boxes
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1892-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1892-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: 00841436120050; Lot Numbers: A174424, A176855, A177208, A182744, A184023, A185336, A185337, A186904, A189734, A190489, A193623, A194755, A198716, A198795, A199940, A200430, A202208, A203169, A203201, A203520, A205457, A207901, A208740, A211619, A212291, A213027, A215531, A216885, A217412, A220102, A221365, A221925, A225145, A226800, A228446, A228778, A229092, A229898, A230045, A230054, A230549, A230581, A231101, A231810, A232903, A233075, A233535, A236538, A238767, A239339, A239355, A240873, A240931, A241445, A242018, A242161, A243263, A243264, A245342, A245527, A246173, A248520, A248572, A250325, A252513, A252842, A254080, A254081, A254900, A254955, A255332, A257534, A258150, A258926, A260607 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

OUS Distribution to countries of: Japan, Taiwan, France, Georgia, Germany and Denmark

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Georgia](https://isitonrecall.com/state/georgia/)

## Dates in the source

- **Report date**: Jun 11, 2025
- **Recall initiation date**: May 1, 2025
- **Center classification date**: May 30, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1892-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Civco Medical Instruments Co. Inc. records](https://isitonrecall.com/brand/civco-medical-instruments-co-inc/)