THOMAS by Gardner Denver — Class II medical device recall Z-2149-2015
Terminated recall by Gardner Denver Thomas Inc, reported 2015-07-29. Vacuum pump may not perform to specification.
| Recall number | Z-2149-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Gardner Denver Thomas Inc, Monroe, LA, United States |
| Recall initiated | 2015-06-04 |
| Classified | 2015-07-20 |
| Reported by FDA | 2015-07-29 |
| Terminated | 2016-08-09 |
| Countries outside the US | CL, CO, MX, MY, PE, SV, VN |
| Quantity | 160 units |
| Serial numbers | 2639-2798 |
| Model numbers | 1240 |
Product
THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1240 Product Usage: medical aspirator
Reason for recall
Vacuum pump may not perform to specification.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2149-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.