FDA Medical Device Recalls (openFDA)
Collagen Matrix Inc: NuOSS Cancellous Intended for use in dental surgery.
- Recall number
- Z-1096-2016
- Recalling firm
- Collagen Matrix Inc
- Product
- NuOSS Cancellous Intended for use in dental surgery.
- Status
- Terminated
- Initiated
- 2015-08-25
- Posted
- not on file
- Terminated
- 2016-05-11
- Reason
- 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.
- Root cause
- Unknown/Undetermined by firm
- Action
- Collagen Matrix Inc. notified their sole customer on November 17, 2015. On August 25, 2015, during a review of inventory, tt was discovered that of the 171 units product shipped, 19 units may have been the incorrect size. For further questions please call (201) 405-1477
- Quantity
- 171 units
- Distribution
- US Distribution to the state of : MA
- Lot, serial or model codes
- Reference No. BM2C20010-U Lot no. BM2CU15E2
- 510(k) numbers
- ["K043034"]
- PMA numbers
- not on file
- Product code
- NPM
- Firm FEI
- 3003300673
- Firm city
- Franklin Lakes
- Firm state
- NJ
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28