Stradis Medical, LLC dba Stradis Healthcare: Medical Device Recall in 2021 - (Recall #: Z-0126-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Tenaculum, Plastic

Product Classification:

Class II

Date Initiated: September 10, 2021

Date Posted: October 27, 2021

Recall Number: Z-0126-2022

Event ID: 88656

Reason for Recall:

Firm unable to confirm that the tenaculum devices were produced in accordance with required design and manufacturing standards.

Status: Ongoing

Product Quantity: 2483 kits

Code Information:

Part Number: 356T

Distribution Pattern:

Distributed nationwide to VA, SC, CA, PA, MA, FL, TN, NJ, GA, AZ, IL, OH, OK, WA, NY, NV, MO, MD, IN, TX, CO, RI, NC, KY, MT, VI, GA, KS, MI, AK, ID, SD, UT and internationally to Canada.

Voluntary or Mandated:

Voluntary: Firm initiated