Reported Jun 25, 2025 · Ongoing

Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in…

Preat Corp.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Preat Corp · 2625 Skyway Dr Ste B · Santa Maria, CA · 93455-1405

Is this the product you have?

  • Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations.
Lot codes and dates
  • Model Number9001767-F
  • UDI-DI code00842092166093
  • Lot Numbers
    • CN932775
    • ED11-202416933
    • ED11-20249907
    • ED11-202435949
    • CN939348
    • ED11-202417239
    • ED11-202411745
    • ED11-202436404
    • CN945176
    • ED11-202419976
    • ED11-202413957
    • ED11-202437437
    • CN946712
    • ED11-202422121
    • ED11-202414696
    • ED11-202437710
    • TEC29015668
    • ED11-202422577
    • ED11-202416838
    • ED11-202437908
    • 29018601
    • ED11-202428254
    • ED11-202433998
    • ED11-202449612
    • RD10511988
    • ED11-202428428
    • ED11-202435120
    • 242070
    • 2905742
    • ED11-20249819
    • ED11-202435909
    • 20-607-UCHE-000603
    • 8-663465-000743
    • 3-16287-002239
    • 14-493GARIEPY-000488
    • 20-769300-000697
    • 20-663461ROBI-000707
    • 30-15958-002006
    • 7-804684-001981
    • 13-766227-000633
    • 6-662469CARM-000576
    • 20-15117-001341
    • 22-790909-001273
    • 8-489686-000448
    • 30-Y097-002143
    • 19-14364-001061
    • 10-788120-001206
    • 7-754951-000206
    • 3-RIEHL-001837
    • CO19-2024-91576
    • CO19-2024-68877
    • CO19-2024-36953
    • CO19-2024-24127
Amount recalled
145 abutments

Where it was sold

Why it was recalled

Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Preat Corp. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:19 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.