Reported Jul 17, 2024 · Ongoing
9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous…
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?
- 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation.
- Lot codes and dates
- Model Number9006767
- UDI-DI code00842092159477
- Lot Numbers
ED11-20247825ED11-20248895ED11-20249165 and 241588
- Amount recalled
- 7 abutmens
Where it was sold
Why it was recalled
Due to incorrect milled titanium abutment being packaged and labeled.
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.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.