Recall Z-1333-2019— Shippert Medical Technologies

Name: FDA recall Z-1333-2019
Creator: U.S. Food and Drug Administration
Published: 2018-02-02

Class II · Completed

Class II FDA medical device recall by Shippert Medical Technologies, initiated 2018-02-02. It names one FDA 510(k) clearance: K092482. Product: Tissu-Trans FILTRON 1000, Catalog 3-TT-FILTRON 1000, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO..

Recalling firm: Shippert Medical Technologies
Classification: Class II
Status: Completed
Initiated: 2018-02-02
Firm location: Centennial, CO, United States

510(k) clearances named in this recall

1 on FDA's record

K092482 — TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500Shippert Medical Technologies Corp.·cleared 2009-12-04

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

Tissu-Trans FILTRON 1000, Catalog 3-TT-FILTRON 1000, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.

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