Drug recall
T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient use, non-sterile prescription…
FDA recall event 73130 · Class II · Salter Labs
Key facts
| Event ID | 73130 |
|---|---|
| Recall numbers | Z-0796-2016 |
| Recalling firm | Salter Labs |
| Product type | Devices |
| Products | T-piece Nebulizer with in-line connectors, Part number 8915-7-50. Single patient use, non-sterile prescription device designed for use in a hospital or home care environment. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Reports that the T-piece does not fit on the nebulizer. |
| Initiation date | Jan 5, 2016 |
| Report date | Feb 17, 2016 |
| Termination date | Apr 21, 2016 |
| City | Carlsbad |
| State | CA |
| Country | United States |
| FEI number | 3000219639 |
At a glance
- 1–9 Products in this recall
- None 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: