Microbiologics Inc: Medical Device Recall in 2022 - (Recall #: Z-0581-2022)

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) 2 Pack Clostridium perfringens derived from ATCC(R) 13124(TM)

Product Classification:

Class III

Date Initiated: October 8, 2020

Date Posted: February 16, 2022

Recall Number: Z-0581-2022

Event ID: 89386

Reason for Recall:

The incorrect lot number was printed on the foil pouch that the KWIK-STIK" is placed in. All foil pouches for lot 318-234-4 have the lot number misprinted as 218-234-4. The correct lot number was printed on the KWIK-STIK" canister label and KWIK-STIK" device label.

Status: Terminated

Product Quantity: 187 units

Code Information:

Catalog Number : 0318P, Lot Number: 318-234-4, UDI: 20845357006213

Distribution Pattern:

US distribution to . International distribution to Austria, Botswana, Brazil, Canada, China, Colombia, Finland, France, Germany, Guatemala, India, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Korea, Republic of, Lithuania, Malaysia, Mauritius, Netherlands, Norway, Oman, Peru, Poland, Romania, South Africa, Switzerland, Taiwan, Thailand, Turkey, United Kingdom, Vietnam

Voluntary or Mandated:

Voluntary: Firm initiated