FDA Medical devices recall ·
Jiffy Original Composite Polisher Cups (Coarse) 12pk recall
- Recall number
- Z-1689-2026
- Date
- (initiated January 28, 2026)
- Company / brand
- Ultradent Products, Inc.
505 W 10200 S, South Jordan, UT, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 2508
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.
Why was it recalled?
Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI-DI: E29270111. Lot: 529983. Expiration: 2031-09-02
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: Alabama Arizona California Connecticut Florida Hawaii Iowa Illinois Kentucky Louisiana Massachusetts Maine Michigan Minnesota Missouri North Carolina Nebraska New Jersey Nevada New York Ohio Oregon Pennsylvania Puerto Rico Texas Utah Virginia Washington Wisconsin West Virginia Wyoming
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1689-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.