---
title: "Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615 — FDA record Z-0727-2023 | Is It on Recall"
description: "The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and vice-versa."
url: https://isitonrecall.com/recall/fda-device-z-0727-2023-corin-biolox-delta-mod-head-036mm-ex-long-8mm-ref-104-3615/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615 — FDA record Z-0727-2023

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 8, 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**: Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615
- **Reason**: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and vice-versa.
- **Classification**: Class II
- **Recalling firm**: Corin Ltd
- **Quantity**: 12 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0727-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0727-2023%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 (01) 0 5055196 96834, Lot 503151 |

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

## Distribution

US Nationwide distribution in the states of FL, GA, MA, MI, Ok, PA, TX.

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

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Nebraska](https://isitonrecall.com/state/nebraska/)
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- [Oregon](https://isitonrecall.com/state/oregon/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
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- [South Carolina](https://isitonrecall.com/state/south-carolina/)
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- [Tennessee](https://isitonrecall.com/state/tennessee/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Dec 28, 2022
- **Recall initiation date**: Nov 8, 2022
- **Center classification date**: Dec 19, 2022

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-0727-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Corin Ltd records](https://isitonrecall.com/brand/corin-ltd/)