FDA Recall Open, Classified

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.

Recall: Z-2318-2024 · Initiated April 10, 2024

Recall

Recall Number
Z-2318-2024
Event Number
94693
Firm
Preat Corp
FEI Number
2918719
Product Code
NHA
Status
Open, Classified
Root Cause
Process control
Initiated
April 10, 2024
Posted
July 8, 2024
Address
2625 Skyway Dr, Ste B, Santa Maria, CA, 93455-1405

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.

Reason

Due to incorrect milled titanium abutment being packaged and labeled.

Action

On 05/21/2024, the firm sent via direct certified mail an "URGENT: MEDICAL DEVICE RECALL UPDATE" Letter to customers informing them that product labeled as part number 9006767-F Astra EV 4.8mm Milled Titanium Abutment may contain instead part number 9006667 Astra EV 4.2mm Milled Titanium Abutment. The potential risk identified was, the screw seat is higher than specified in the engineering drawings and required for full thread engagement with the implant. This condition reduces the screw thread engagement with the implant. Customer are instructed to: Product in the scope of this recall shall be discarded or returned to PREAT CORPORATION. Instructions for the return will be provided. All personnel within your company should be made aware of the issue. Any customers to which this product has been further distributed should be notified. For questions or assistance contact Jose Espino at 224-622-7191 or email [email protected]

Distribution

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

Quantity

7 abutmens