FDA recall record

Nobel Biocare Procera NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25 s2 - Product Usage: Implant Crown recall — FDA Z-1677-2021

Not manufactured to specification

Class IIclassification
Z-1677-2021official record ID
Jun 2, 2021report date

Recall record at a glance

Official recordZ-1677-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNobel Biocare Procera LLC
Report dateJun 2, 2021
Recall initiation dateMar 29, 2021
Quantity2 units
LocationMahwah, NJ, United States

Official product description

NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25 s2 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics Material Number: 77339

Why the product was recalled

Not manufactured to specification

Distribution information

Worldwide distribution - US Nationwide distribution in the states of AL,CA, OK, WA and the countries of Belgium, Canada, Italy, Sweden, Switzerland.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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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