FDAClass IIMarch 23, 2016

NuOSS Cancellous Intended for use in dental surgery recall

NuOSS Cancellous Intended for use in dental surgery.

Why was NuOSS Cancellous Intended for use in dental surgery 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.

What should I do if I have this product?

Review the official FDA enforcement record for current 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?

Reference No. BM2C20010-U Lot no. BM2CU15E2

Product
NuOSS Cancellous Intended for use in dental surgery.
Recalling firm
Collagen Matrix Inc
Quantity
171 units
Distribution
US Distribution to the state of : MA
Recall date
March 23, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls