Recall Z-3061-2017— Shippert Medical Technologies

Class II · Terminated

Class II FDA medical device recall by Shippert Medical Technologies, initiated 2017-06-01, terminated 2024-01-30. FDA's recall record names no specific 510(k) clearance for this event. Product: Tissu-Trans Filtron 250, 3-TT-FILTRON 250. Product Usage: Intended for fat transfer and liposuction.. Reason: Seal integrity of the Tissu-Trans product sterile packages cannot be assured..

Recalling firm
Shippert Medical Technologies
Classification
Class II
Status
Terminated
Initiated
2017-06-01
Terminated
2024-01-30
Firm location
Centennial, CO, United States

Product description

Tissu-Trans Filtron 250, 3-TT-FILTRON 250. Product Usage: Intended for fat transfer and liposuction.

Reason for recall

Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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