Recall of Jiffy Original Composite Polisher Cups
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Ultradent Products, Inc. is voluntarily recalling 2508 units of Jiffy Original Composite Polisher Cups due to potential crumbling that could delay patient treatment.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 15, 2026 and geographically references United States. Its severity classification of "low" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
Recall of Jiffy Original Composite Polisher Cups
What Happened
Ultradent Products, Inc. is recalling the product because the composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.
Which Products Are Affected
The affected product is Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011. A total of 2508 units are involved, with the following details: UDI-DI: E29270111, Lot: 529983, and Expiration: 2031-09-02. The products were distributed to the following US states and territories: 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. The recall number is Z-1689-2026.
What You Should Do
For information on this recall, refer to the FDA recall notice or contact the recalling firm, Ultradent Products, Inc., as it is a voluntary firm-initiated recall.
Why This Matters
This recall involves a potential issue that could delay dental procedures, affecting patient care in the United States.
Source
FDA recall notice Z-1689-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,083 characters here).
Similar severity timing
Same severity (low) notices issued closest in time to April 15, 2026.
Frequently Asked Questions
Common questions about this FDA recall.