Drug recall
KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.
FDA recall event 86178 · Class II · Cardinal Health 200, LLC
Key facts
| Event ID | 86178 |
|---|---|
| Recall numbers | Z-3016-2020 |
| Recalling firm | Cardinal Health 200, LLC |
| Product type | Devices |
| Products | KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Only providing one nasal swab in our pre-operative kit instead of the 4 required for proper treatment. |
| Initiation date | Jul 30, 2020 |
| Report date | Oct 7, 2020 |
| Termination date | Apr 28, 2021 |
| City | Fort Mill |
| State | SC |
| Country | United States |
| FEI number | 3002973487 |
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: