Collagen Matrix Inc: Medical Device Recall in 2016 - (Recall #: Z-1096-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

NuOSS Cancellous Intended for use in dental surgery.

Product Classification:

Class II

Date Initiated: August 25, 2015

Date Posted: March 23, 2016

Recall Number: Z-1096-2016

Event ID: 73222

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.

Status: Terminated

Product Quantity: 171 units

Code Information:

Reference No. BM2C20010-U Lot no. BM2CU15E2

Distribution Pattern:

US Distribution to the state of : MA

Voluntary or Mandated:

Voluntary: Firm initiated