---
title: "Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHI... — FDA record Z-0958-2023 | Is It on Recall"
description: "Reaction vessels may contain a potential contaminant that could affect their optical performance."
url: https://isitonrecall.com/recall/fda-device-z-0958-2023-alinity-reaction-vessels-ref-06p1401-for-use-with-alinity-i-systems-architect-reaction-vessels/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels — FDA record Z-0958-2023

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 Nov 24, 2022. 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**: Alinity Reaction Vessels, REF: 06P1401, for use with Alinity i Systems; ARCHITECT Reaction Vessels
- **Reason**: Reaction vessels may contain a potential contaminant that could affect their optical performance.
- **Classification**: Class III
- **Recalling firm**: Abbott Laboratories
- **Quantity**: 70 cases
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0958-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0958-2023%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/Lots: 00380740129026/000586790 and 000586879 |

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

## Distribution

US Distribution: IL, MN, MO, NC, ND, NJ, NY, OK, SC, TX, WV

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

- [Illinois](https://isitonrecall.com/state/illinois/)
- [Minnesota](https://isitonrecall.com/state/minnesota/)
- [Missouri](https://isitonrecall.com/state/missouri/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [North Dakota](https://isitonrecall.com/state/north-dakota/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
- [Texas](https://isitonrecall.com/state/texas/)
- [West Virginia](https://isitonrecall.com/state/west-virginia/)

## Dates in the source

- **Report date**: Jan 25, 2023
- **Recall initiation date**: Nov 24, 2022
- **Center classification date**: Jan 17, 2023

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-0958-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Abbott Laboratories records](https://isitonrecall.com/brand/abbott-laboratories/)