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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Jiffy Original Composite Polisher Cups Recalled for Crumbling Risk

Agency Publication Date: March 27, 2026
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Summary

Ultradent Products, Inc. is recalling 2,508 units of Jiffy Original Composite Polisher Cups (Coarse) because the cups may crumble and break apart easily during dental procedures. This defect can lead to interruptions or delays in patient treatment while the clinician addresses the failing equipment. The recall affects 12-pack containers of the coarse variety, identified by model REF 7011, which were distributed to 31 U.S. states and Puerto Rico.

Risk

The polisher cups can disintegrate during use, which may cause a delay in dental treatment or require the clinician to clear debris from the patient's mouth.

What You Should Do

  1. Identify the affected product by checking the packaging for 'Jiffy Original Composite Polisher Cups (Coarse) 12pk' with model number REF 7011.
  2. Check for lot number 529983 and an expiration date of 2031-09-02, which is printed on the product label.
  3. Stop using the recalled product immediately.
  4. Contact Ultradent Products, Inc. or your dental supply distributor to arrange for a return, replacement, or correction.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional questions.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Jiffy Original Composite Polisher Cups (Coarse) 12pk
Variants: Coarse
Model / REF:
7011
Lot Numbers:
529983 (Exp 2031-09-02)
UDI:
E29270111

Quantity affected: 2508 units.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98419
Status: Active
Manufacturer: Ultradent Products, Inc.
Sold By: Dental supply distributors
Manufactured In: United States
Units Affected: 2508
Distributed To: Massachusetts, Wisconsin, Maine, Alabama, New York, Minnesota, California, Kentucky, Illinois, Wyoming, Washington, Ohio, Puerto Rico, Connecticut, Oregon, New Jersey, Michigan, North Carolina, Hawaii, Pennsylvania, Nebraska, Texas, Utah, Nevada, Louisiana, Virginia, Missouri, Florida, Arizona, West Virginia, Iowa

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.