Drug recall
Bacterin International, Inc., Osteoselect Demineralized Bone Matrix DMB Putty; Graft ID# B090056-664 Donor#…
FDA recall event 63433 · Class II · Bacterin International, Inc.
Key facts
| Event ID | 63433 |
|---|---|
| Recall numbers | Z-0800-2013 |
| Recalling firm | Bacterin International, Inc. |
| Product type | Devices |
| Products | Bacterin International, Inc., Osteoselect Demineralized Bone Matrix DMB Putty; Graft ID# B090056-664 Donor# B090056 2.5cc Expiration Date: 12/25/2011; LBL 210-0010-1 REV: 040109; and Graft ID#… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Expired product was shipped to two customers. |
| Initiation date | Apr 18, 2012 |
| Report date | Feb 20, 2013 |
| Termination date | May 13, 2013 |
| City | Belgrade |
| State | MT |
| Country | United States |
| FEI number | 3005168462 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: