---
title: "Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011. — FDA record Z-1689-2026 | Is It on Recall"
description: "Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment."
url: https://isitonrecall.com/recall/fda-device-z-1689-2026-jiffy-original-composite-polisher-cups-coarse-12pk-ref-7011/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011. — FDA record Z-1689-2026

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 28, 2026. 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**: Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.
- **Reason**: Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.
- **Classification**: Class II
- **Recalling firm**: Ultradent Products, Inc.
- **Quantity**: 2508
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1689-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1689-2026%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: E29270111. Lot: 529983. Expiration: 2031-09-02 |

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

## Distribution

US: MA, WI, ME, AL, NY, MN, CA, KY, IL, WY, WA, OH, PR, CT, OR, NJ, MI, NC, HI, PA, NE, TX, UT, NV, LA, VA, MO, FL, AZ, WV, IA.

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

- [Alabama](https://isitonrecall.com/state/alabama/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Apr 8, 2026
- **Recall initiation date**: Jan 28, 2026
- **Center classification date**: Mar 27, 2026

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-1689-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Ultradent Products, Inc. records](https://isitonrecall.com/brand/ultradent-products-inc/)