Microbiologics Inc: Medical Device Recall in 2022 - (Recall #: Z-0641-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

KWIK-STIK(TM), Quality control kit for culture media, sold as: KWIK-STIK(TM) 2-pack Enterococcus faecalis derived from ATCC(R) 51299(TM)

Product Classification:

Class III

Date Initiated: March 25, 2013

Date Posted: February 23, 2022

Recall Number: Z-0641-2022

Event ID: 89479

Reason for Recall:

Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7, contained an inner label stating the product is Catalog #0919K Haemophilus influenza. The organism has been confirmed to be C. coli, indicating this is a labeling error and the organism is the correct organism.

Status: Terminated

Product Quantity: 10 units

Code Information:

Catalog Number 01023P, UDI: 20845357029502, Lot Number (Expiration Date): 1023-05-7 (04/30/2014)

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Canada, South Africa, France, Netherlands, Mauritius, China.

Voluntary or Mandated:

Voluntary: Firm initiated