Drug recall
Achilles Tendon
FDA recall event 25676 · Class I · Cryolife Inc
Key facts
| Event ID | 25676 |
|---|---|
| Recall numbers | B-0941-3, B-0942-3, B-0943-3, B-0944-3, B-0945-3 |
| Recalling firm | Cryolife Inc |
| Product type | Biologics |
| Products | Achilles Tendon, Hemi Patellar Tendon, Saphenous veins, Semi-quadriceps Tendon, Tibialis Tendon |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Human tissues for transplantation was positve for microorganisms, were distributed., Human tissues for transplantationwas positve for microorganisms, were distributed. |
| Initiation date | Feb 4, 2003 |
| Termination date | Aug 9, 2004 |
| City | Kennesaw |
| Country | United States |
| FEI number | 3001451326 |
At a glance
- 1–9 Products in this recall
- 10–99 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