PlainRecalls
FDA Devices Moderate Class II Terminated

NuOSS Cancellous Intended for use in dental surgery.

Reported: March 23, 2016 Initiated: August 25, 2015 #Z-1096-2016

Product Description

NuOSS Cancellous Intended for use in dental surgery.

Reason for Recall

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.

Details

Recalling Firm
Collagen Matrix Inc
Units Affected
171 units
Distribution
US Distribution to the state of : MA
Location
Franklin Lakes, NJ

Frequently Asked Questions

What product was recalled?
NuOSS Cancellous Intended for use in dental surgery.. Recalled by Collagen Matrix Inc. Units affected: 171 units.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 23, 2016. Severity: Moderate. Recall number: Z-1096-2016.