Recall Z-2150-2015— Gardner Denver Thomas Inc

Name: FDA recall Z-2150-2015
Creator: U.S. Food and Drug Administration
Published: 2015-06-04

Class II · Terminated

Class II FDA medical device recall by Gardner Denver Thomas Inc, initiated 2015-06-04, terminated 2016-08-09. It names one FDA 510(k) clearance: K965059. Product: THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1242 Product Usage: medical aspirator. Reason: Vacuum pump may not perform to specification..

Recalling firm: Gardner Denver Thomas Inc
Classification: Class II
Status: Terminated
Initiated: 2015-06-04
Terminated: 2016-08-09
Firm location: Monroe, LA, United States

510(k) clearances named in this recall

1 on FDA's record

K965059 — CPI, MAXI-VAC(6480),THOMAS INDUSTRIES, MEDI-PUMP(1240/1242/1243)Thomas Industries·cleared 1997-03-04

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1242 Product Usage: medical aspirator

Reason for recall

Vacuum pump may not perform to specification.

Data sourced from openFDA. This site is unofficial and independent of the FDA.