FDAClass IIMarch 27, 2024

Preat Nobel Active/Conical-compatible RP Titanium Blank recall

Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967

Why was Preat Nobel Active/Conical-compatible RP Titanium Blank recalled?

Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Model Number: 9000967 UDI-DI code: 00842092165867 Lot Numbers: 235650, 234294, 233667, 233885, 233439, and 231489

Product
Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
Recalling firm
Preat Corp
Quantity
561 units
Distribution
U.S. Nationwide distribution in the states of AZ, OH and PA.
Recall date
March 27, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls