Sybron recalls Drill Stop Kit with incorrect components that may affect sterilization and safety. Affected units include specific lot numbers for sterilizable trays used in dental procedures.
“Sybron Drill Stop Kit Recall: Incorrect Components Hazard.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52359-sybron-drill-stop-kit-recall-incorrect-components-hazard. Based on FDA recall #Z-2172-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2172-2025%22&limit=1).
The FDA announced on May 1, 2025, that Implant Direct Sybron Manufacturing LLC is recalling The Drill Stop Kit due to incorrect components. GovInfoNow's records show this voluntary Class II recall affects 45 kits distributed worldwide.
How to tell if you have it
Brand: Sybron
Product: The Drill Stop Kit (version of the Mini Sterilizable Tray)
Lot #: 15006511
UDI: (10)841307125310
The hazard
The Drill Stop Kit contains incorrect components. The kit is used to store, sterilize, and verify Drill Stop length via a ruler and depth markings.
Context
GovInfoNow's records show Implant Direct Sybron Manufacturing LLC has 20 other recalls on record since June 26, 2017. Other recent recalls of similar products include Medline Convenience Kits Recall: Calibration Issues May Affect Sterility (Jan. 7, 2026) and Medline Convenience Kits Recall: Sterility Risk from Calibration Issues (Jan. 7, 2026).
How to tell if you have this one
Check for lot number 15006511/UDI: (10)841307125310 on the Drill Stop Kit. The product is a sterilizable tray used in dental procedures to store and verify Drill Stops.
Brand
Sybron
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Lot Number
Look for lot number 15006511/UDI: (10)841307125310 on the Drill Stop Kit.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 13 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide - US Nationwide distribution in the states of AL, FL, LA, MD, NJ, NV, NY, OH, OK, TN, TX, UT, VA and the country of Japan.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Florida, Louisiana, Maryland, Nevada, New Jersey, New York, Ohio, Oklahoma, Tennessee, Texas, Utah, Virginia.
Recall timeline
FDA published this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2172-2025 (May 1, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2172-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.