FDA recall record

Preat 9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in recall — FDA Z-2318-2024

Due to incorrect milled titanium abutment being packaged and labeled.

Class IIclassification
Z-2318-2024official record ID
Jul 17, 2024report date

Recall record at a glance

Official recordZ-2318-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmPreat Corp
Report dateJul 17, 2024
Recall initiation dateApr 10, 2024
Quantity7 abutmens
LocationSanta Maria, CA, United States

Official product description

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.

Why the product was recalled

Due to incorrect milled titanium abutment being packaged and labeled.

Distribution information

U.S.: CA, MO, and NV. O.U.S.: None

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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