Microbiologics Inc: Medical Device Recall in 2023 - (Recall #: Z-0307-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

KWIKSTIK, P. venetum, Catalog numbers: a) 0794P (2-pack), b) 0794K (6-pack)

Product Classification:

Class II

Date Initiated: October 18, 2023

Date Posted: November 22, 2023

Recall Number: Z-0307-2024

Event ID: 93267

Reason for Recall:

A complaint investigation showed that the bulk pellets (lot 794-142) were contaminated with Aspergillus flavus.

Status: Ongoing

Product Quantity: 13 units

Code Information:

a) UDI/DI 20845357019169, Lot Numbers: 794-142-2, 794-142-4 b) UDI/DI 30845357019173, Lot Numbers: 794-142-3

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Italy, France, Turkey, Peru, Mexico.

Voluntary or Mandated:

Voluntary: Firm initiated