FDA recall record

Nobel Biocare Usa Instructions for Use (IFU) and Manual NobPrl CC Guided Surgery Kit recall — FDA Z-2375-2016

Incorrect drill protocol in the Instructions for Use (IFU)

Class IIclassification
Z-2375-2016official record ID
Aug 17, 2016report date

Recall record at a glance

Official recordZ-2375-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNobel Biocare Usa LLC
Report dateAug 17, 2016
Recall initiation dateJul 20, 2016
Quantity231 kits
LocationYorba Linda, CA, United States

Official product description

Instructions for Use (IFU) and Manual NobPrl CC Guided Surgery Kit Instructions for Use (IFU): "NobelGuide for NobelParallel Conical Connection", id # 2002 and Manual: Guided Surgery with NobelParallel Conical Connection", id # 79423. Article # 38072, Nobel Parallel CC Guided Surgery Kit. The Guided Surgery Kit is used as part of the installation process of NobelParallel CC Implants. The purpose of the IFU is to instruct the user how to use the products safely. The purpose of the manual is to guide the user through the usage of NobelGuide for NobelParallel CC.

Why the product was recalled

Incorrect drill protocol in the Instructions for Use (IFU)

Distribution information

Worldwide Distribution: US (nationwide) and Countries of: Austria, Belgium, Canada, Germany, Denmark, Spain, France, Great Britain, Italy, Netherlands, Norway, Poland, Portugal, Russia, and Turkey.

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

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About this record

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