---
title: "Irvine Scientific Oil for Embryo Culture (Light Mineral Oil) REF Catalog # 9305 — FDA record Z-1314-2023 | Is It on Recall"
description: "Due to the detection of oil toxicity in several lots of Oil for Embryo Culture products."
url: https://isitonrecall.com/recall/fda-device-z-1314-2023-irvine-scientific-oil-for-embryo-culture-light-mineral-oil-ref-catalog-9305/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Irvine Scientific Oil for Embryo Culture (Light Mineral Oil) REF Catalog # 9305 — FDA record Z-1314-2023

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 Jan 16, 2023. 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**: Irvine Scientific Oil for Embryo Culture (Light Mineral Oil) REF Catalog # 9305
- **Reason**: Due to the detection of oil toxicity in several lots of Oil for Embryo Culture products.
- **Classification**: Class II
- **Recalling firm**: Fujifilm Irvine Scientific, Inc.
- **Quantity**: 15,131 bottles
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1314-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1314-2023%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 Code: 08937270029305TH Catalog Number / Lot Numbers: 9305-100ml / 0000011351, 9305-500ml / 0000011367, 9305-100ml / 0000015999, 9305-500ml / 0000016001 |

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

## Distribution

U.S.: AZ, AR, CA, CT, DC, FL, HI, IA, ID, IL, IN, KS, MA, MD, ME, MI, MN, MO, NC, NE, NH, NJ, NV, NY, OH, OK, PA, RI, SC, TN, TX, UT, VA, WI and WV. O.U.S.: India, Israel, Japan, Malaysia, Mexico, South Korea, South Africa, Thailand, Vietnam, Brazil, Bosnia, Argentina, Netherlands, and United Kingdom

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

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## Dates in the source

- **Report date**: Apr 5, 2023
- **Recall initiation date**: Jan 16, 2023
- **Center classification date**: Mar 30, 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-1314-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Fujifilm Irvine Scientific, Inc. records](https://isitonrecall.com/brand/fujifilm-irvine-scientific-inc/)