---
title: "Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023, REF 001156T0), carbide... — FDA record Z-1008-2024 | Is It on Recall"
description: "The device has a grip detail (right angle latch) out of specification causing the bur to not adequately latch in the handpiece."
url: https://isitonrecall.com/recall/fda-device-z-1008-2024-brasseler-8s-ra-shp-rd-super-sharp-round-h1s-21-023-ref-001156t0-carbide-dental-bur-10-burs-package/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023, REF 001156T0), carbide dental bur, 10 burs/package, Rx. — FDA record Z-1008-2024

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 11, 2024. 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**: Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023, REF 001156T0), carbide dental bur, 10 burs/package, Rx.
- **Reason**: The device has a grip detail (right angle latch) out of specification causing the bur to not adequately latch in the handpiece.
- **Classification**: Class II
- **Recalling firm**: Brasseler USA I Lp
- **Quantity**: 440 burs
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1008-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1008-2024%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 | Lot numbers L01G6 and L16P9, UDI-DI 00887919188483, RX. |

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

## Distribution

Worldwide - US Nationwide distribution in the states of AL, CA, CO, DC, IL, NY, OH, OR, PA, TN, TX, and WA. The country of Canada.

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**: Feb 14, 2024
- **Recall initiation date**: Jan 11, 2024
- **Center classification date**: Feb 7, 2024

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-1008-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Brasseler USA I Lp records](https://isitonrecall.com/brand/brasseler-usa-i-lp/)
