Shippert Medical Technologies: Medical Device Recall in 2017 - (Recall #: Z-3062-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Tissu-Trans Filtron 500, 3-TT-FILTRON 500. Product Usage: Intended for fat transfer and liposuction.

Product Classification:

Class II

Date Initiated: June 1, 2017

Date Posted: August 30, 2017

Recall Number: Z-3062-2017

Event ID: 77518

Reason for Recall:

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

Status: Terminated

Product Quantity: 5,188 units total

Code Information:

Lot Numbers 11934, 11948, 11984, 12002, 12020, 12046, 61119, 61287, 61363, 61146.

Distribution Pattern:

Worldwide Distribution - US Nationwide in the states of: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, KY, MD, MI, MN, MO, NC, NJ, NV, NY, OH, OR, PA, TN, TX, UT, VA, WA, WV. and the countries of: Italy, Austria, Turkey, United Arab Emirates, Germany, Spain, Saudi Arabia, Switzerland, Japan Kuwait, Denmark, Sweden, United Kingdom, Belgium, France, Australia, Netherlands, Greece, South Korea.

Voluntary or Mandated:

Voluntary: Firm initiated