---
title: "API ID 32 C Strips, Reference 32200, Rx Only, IVD API ID 32 C is a qualitativ... — FDA record Z-0525-2022 | Is It on Recall"
description: "Risk of misidentification or delayed results with the absence of identification due to thermoforming defect."
url: https://isitonrecall.com/recall/fda-device-z-0525-2022-api-id-32-c-strips-reference-32200-rx-only-ivd-api-id-32-c-is-a-qualitative-standardized-system-for/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# API ID 32 C Strips, Reference 32200, Rx Only, IVD API ID 32 C is a qualitative standardized system for the identifica... — FDA record Z-0525-2022

Reported terminated

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 Dec 20, 2021. 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**: API ID 32 C Strips, Reference 32200, Rx Only, IVD API ID 32 C is a qualitative standardized system for the identification of yeasts. It uses miniaturized tests as well as a specially adapted database. After manual inoculation of the strip, reading can be performed either automatically or manually and the identification is obtained using an identification software.
- **Reason**: Risk of misidentification or delayed results with the absence of identification due to thermoforming defect.
- **Classification**: Class II
- **Recalling firm**: Biomerieux Inc
- **Quantity**: 462 kits
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0525-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0525-2022%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 | Model No. 32200; Lot 1008781060. |

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

## Distribution

US (Domestic) Distribution to states of: AZ, IA, KY, and NY.

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

- [Arizona](https://isitonrecall.com/state/arizona/)
- [Iowa](https://isitonrecall.com/state/iowa/)
- [Kentucky](https://isitonrecall.com/state/kentucky/)
- [New York](https://isitonrecall.com/state/new-york/)

## Dates in the source

- **Report date**: Feb 2, 2022
- **Recall initiation date**: Dec 20, 2021
- **Center classification date**: Jan 25, 2022
- **Termination date**: Sep 25, 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-0525-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Biomerieux Inc records](https://isitonrecall.com/brand/biomerieux-inc/)