THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1240 Product Usage: medical aspirator
FDA Recall Z-2149-2015 · Posted 2015-07-20
Recalling FirmGardner Denver Thomas Inc
Recall StatusTerminated
Product CodeJCX
Date Initiated2015-06-04
Date Terminated2016-08-09
Product Quantity160 units
Reason for Recall
Vacuum pump may not perform to specification.
Firm Action
Gardner Denver Thomas sent an Important Medical Device Recall letter dated May 7, 2015 to affected distributors. The letter identified the affected products, problem and actions to be taken. For questions call your Customer Service Representative or Sales Representative or the Recall Coordinator at 920-451-6423.
Root Cause
Nonconforming Material/Component
Distribution Pattern
Internationally Distributed in the countries of :Mexico, Peru, El Salvador, Chile, Colombia, Vietnam, and Malaysia.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.