Drug recall
THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1240 Product Usage: medical aspirator
FDA recall event 71569 · Class II · Gardner Denver Thomas Inc
Key facts
| Event ID | 71569 |
|---|---|
| Recall numbers | Z-2149-2015, Z-2150-2015, Z-2151-2015 |
| Recalling firm | Gardner Denver Thomas Inc |
| Product type | Devices |
| Products | THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1240 Product Usage: medical aspirator, THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1242 Product Usage: medical aspirator, THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1243 Product Usage: medical aspirator |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Vacuum pump may not perform to specification. |
| Initiation date | Jun 4, 2015 |
| Report date | Jul 29, 2015 |
| Termination date | Aug 9, 2016 |
| City | Monroe |
| State | LA |
| Country | United States |
| FEI number | 3007725233 |
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: