FDA recall record

Collagen Matrix NuOSS Cancellous Intended for use in dental surgery recall — FDA Z-1096-2016

On 8/25/2015, Collagen Matrix, Inc discovered that one of the 171 units of NuOss Cancellous product shipped to a distributor may have included an…

Class IIclassification
Z-1096-2016official record ID
Mar 23, 2016report date

Recall record at a glance

Official recordZ-1096-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCollagen Matrix Inc.
Report dateMar 23, 2016
Recall initiation dateAug 25, 2015
Quantity171 units
LocationFranklin Lakes, NJ, United States

Official product description

NuOSS Cancellous Intended for use in dental surgery.

Why the product was recalled

On 8/25/2015, Collagen Matrix, Inc discovered that one of the 171 units of NuOss Cancellous product shipped to a distributor may have included an incorrect size.

Distribution information

US Distribution to the state of : MA

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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