FDA Device recall Z-0752-2019
Porcine Anorganic Bone Mineral 4.0cc
- FDA Device
- Class III
- terminated
- Published 2019-01-23
On 2019-01-23 the FDA classified a Class III recall of Porcine Anorganic Bone Mineral 4.0cc by Collagen Matrix, citing there is a possibility that the product labeled as 4.0cc volume may only contain 2.0cc volume and is therefore mislabeled.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0752-2019 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2018-10-30 |
| Published | 2019-01-23 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Collagen Matrix |
| Distribution | FL, TX |
Product
Porcine Anorganic Bone Mineral 4.0cc
Reason
There is a possibility that the product labeled as 4.0cc volume may only contain 2.0cc volume and is therefore mislabeled.
Identifiers
| code_info | UDI - (01)00813954022369(17)210430(10)PMCU18C4 Lot Number - PMCU18C4 Expiration Date - 04/30/2021 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0752-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.