Shippert Medical Technologies: Medical Device Recall in 2019 - (Recall #: Z-1332-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Tissu-Trans FILTRON 500, Catalog 3-TT-FILTRON 500, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.

Product Classification:

Class II

Date Initiated: February 2, 2018

Date Posted: May 22, 2019

Recall Number: Z-1332-2019

Event ID: 81837

Reason for Recall:

The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.

Status: Completed

Product Quantity: 6,553 units were distributed for all catalog numbers

Code Information:

Lot numbers 61508, 61636, 61683, 61753, 61804, 61812, 61813, 61814, 61815, 61862, 61917, 61949, 61991, 62052, 62089, 62134, and 62156

Distribution Pattern:

Distribution was nationwide, including PR. There was government/military distribution. Foreign distribution was made to Australia, Austria, Belgium, Denmark, Germany, Greece, India, Italy, Japan, Netherlands, New Zealand, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and United Kingdom,

Voluntary or Mandated:

Voluntary: Firm initiated