CLASS II ONGOING Device recall · Reported 8 Apr 2026 · FDA Enforcement Report
Jiffy Original Composite Polisher Cups (Coarse) recalled
Ultradent Products is recalling Jiffy Original Composite Polisher Cups (Coarse), distributed in 31 states. The recall was initiated on 28 Jan 2026 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1689-2026
- FDA event ID
- 98419
- Recalling firm
- Ultradent Products, South Jordan, UT
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 28 Jan 2026
- FDA classified
- 27 Mar 2026
- Reported
- 8 Apr 2026
- Type
- Voluntary: Firm initiated
- Reason category
- Device Malfunction
- Device type
- Other Medical Devices
Timeline
| 28 Jan 2026 | Recall initiated by company | |
| 27 Mar 2026 | Classified by FDA | +58 days |
| 8 Apr 2026 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.
Where it was distributed
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.
AlabamaArizonaCaliforniaConnecticutFloridaHawaiiIowaIllinoisKentuckyLouisianaMassachusettsMaineMichiganMinnesotaMissouriNorth CarolinaNebraskaNew JerseyNevadaNew York
Questions about this recall
Why was it recalled?
Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.
Which lots are affected?
UDI-DI: E29270111. Lot: 529983. Expiration: 2031-09-02
Where was it sold?
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.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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